CS196429B2 - Herbicide - Google Patents

Herbicide Download PDF

Info

Publication number: CS196429B2
Authority: CS; Czechoslovakia
Prior art keywords: carbon atoms; align; weight; parts; phenyl
Prior art date: 1977-06-03

Application number

CS783577A

Other languages

Czech (cs)

English (en)

Inventor

Ulrich Schirmer

Bruno Wuerzer

Wolfgang Rohr

Original Assignee

Basf Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-06-03

Filing date

1978-06-01

Publication date

1980-03-31

1978-06-01 Application filed by Basf Ag filed Critical Basf Ag

1980-03-31 Publication of CS196429B2 publication Critical patent/CS196429B2/cs

Links

230000002363 herbicidal effect Effects 0.000 title claims description 11
239000004009 herbicide Substances 0.000 title description 5
125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 28
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 22
125000000217 alkyl group Chemical group 0.000 claims abstract description 12
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 7
229910052736 halogen Inorganic materials 0.000 claims abstract description 7
229910052717 sulfur Inorganic materials 0.000 claims abstract description 7
239000011593 sulfur Substances 0.000 claims abstract description 7
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 6
229910052760 oxygen Inorganic materials 0.000 claims abstract description 6
239000001301 oxygen Substances 0.000 claims abstract description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 4
125000003545 alkoxy group Chemical group 0.000 claims abstract 4
125000000304 alkynyl group Chemical group 0.000 claims abstract 2
150000001602 bicycloalkyls Chemical group 0.000 claims abstract 2
-1 methoxy, cyclohexyl Chemical group 0.000 claims description 87
239000000203 mixture Substances 0.000 claims description 23
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
239000004480 active ingredient Substances 0.000 claims description 11
239000007787 solid Substances 0.000 claims description 6
229910052799 carbon Inorganic materials 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims 2
239000007788 liquid Substances 0.000 claims 1
150000002367 halogens Chemical class 0.000 abstract description 5
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract description 4
239000001257 hydrogen Substances 0.000 abstract description 3
229910052739 hydrogen Inorganic materials 0.000 abstract description 3
125000004122 cyclic group Chemical group 0.000 abstract description 2
125000001188 haloalkyl group Chemical group 0.000 abstract 2
125000003342 alkenyl group Chemical group 0.000 abstract 1
125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
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YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
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238000006243 chemical reaction Methods 0.000 description 15
239000000047 product Substances 0.000 description 15
239000000243 solution Substances 0.000 description 14
239000002253 acid Substances 0.000 description 13
239000013543 active substance Substances 0.000 description 13
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238000000354 decomposition reaction Methods 0.000 description 4
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239000002184 metal Substances 0.000 description 4
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
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UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
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YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
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ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 3
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125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
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238000005984 hydrogenation reaction Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
210000002414 leg Anatomy 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
231100001184 nonphytotoxic Toxicity 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
239000004533 oil dispersion Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000011197 perejil Nutrition 0.000 description 1
GEOWCLRLLWTHDN-UHFFFAOYSA-N phenyl formate Chemical compound O=COC1=CC=CC=C1 GEOWCLRLLWTHDN-UHFFFAOYSA-N 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
239000001739 pinus spp. Substances 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
229920003124 powdered cellulose Polymers 0.000 description 1
235000019814 powdered cellulose Nutrition 0.000 description 1
230000000644 propagated effect Effects 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
235000014774 prunus Nutrition 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000000376 reactant Substances 0.000 description 1
YPSUCTSXOROPBS-UHFFFAOYSA-N s-methyl chloromethanethioate Chemical compound CSC(Cl)=O YPSUCTSXOROPBS-UHFFFAOYSA-N 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000009987 spinning Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
235000011150 stannous chloride Nutrition 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002641 tar oil Substances 0.000 description 1
RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 1
150000003606 tin compounds Chemical class 0.000 description 1
AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
150000003673 urethanes Chemical class 0.000 description 1

Classifications

- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L25/00—Assemblies consisting of a plurality of semiconductor or other solid state devices
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/32—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C271/38—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
- C07C2603/58—Ring systems containing bridged rings containing three rings
- C07C2603/60—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members
- C07C2603/62—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members containing three- or four-membered rings
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Landscapes

Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Environmental Sciences (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Microelectronics & Electronic Packaging (AREA)
Physics & Mathematics (AREA)
Computer Hardware Design (AREA)
Power Engineering (AREA)
General Physics & Mathematics (AREA)
Condensed Matter Physics & Semiconductors (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Polyurethanes Or Polyureas (AREA)

CS783577A 1977-06-03 1978-06-01 Herbicide CS196429B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772725146 DE2725146A1 (de)	1977-06-03	1977-06-03	Diurethane und herbizide

Publications (1)

Publication Number	Publication Date
CS196429B2 true CS196429B2 (en)	1980-03-31

Family

ID=6010672

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS783577A CS196429B2 (en)	1977-06-03	1978-06-01	Herbicide

Country Status (24)

Country	Link
EP (1)	EP0000030B1 (da)
JP (1)	JPS543038A (da)
AT (1)	AT358869B (da)
AU (1)	AU519196B2 (da)
BR (1)	BR7803528A (da)
CA (1)	CA1110264A (da)
CS (1)	CS196429B2 (da)
DD (1)	DD135853A5 (da)
DE (2)	DE2725146A1 (da)
DK (1)	DK247278A (da)
ES (1)	ES470367A1 (da)
FI (1)	FI781762A (da)
HU (1)	HU177551B (da)
IE (1)	IE46905B1 (da)
IL (1)	IL54779A (da)
IT (1)	IT1104710B (da)
NO (1)	NO781931L (da)
NZ (1)	NZ187460A (da)
PL (1)	PL106564B1 (da)
PT (1)	PT68091A (da)
SU (1)	SU725541A3 (da)
TR (1)	TR20048A (da)
YU (1)	YU132578A (da)
ZA (1)	ZA783163B (da)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3113449A1 (de) *	1981-04-03	1982-11-11	Hoechst Ag, 6000 Frankfurt	"thiocarbaminsaeureester, verfahren zu ihrer herstellung, sie enthaltende arzneimittel und ihre verwendung"
JPS5951205A (ja) *	1982-06-23	1984-03-24	Toyo Soda Mfg Co Ltd	カ−バメ−ト誘導体を含有する除草剤
DE19800531A1 (de) *	1998-01-09	1999-07-15	Bayer Ag	Verfahren zur Herstellung von N-(3-Amino-4-fluor-phenyl)-sulfonsäureamiden, N-(3-Amino-4-fluor-phenyl)-carbonsäureamiden und N-(3-Amino-4-fluor-phenyl)-carbamaten

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT1037578B (it) *	1975-04-23	1979-11-20	Snam Progetti	Procedimento per la sintesi di esteri di acidi tiocarbammici
JPS537474A (en) *	1976-07-12	1978-01-23	Tsuneto Yoshii	Process for producing soil conditioner and fertilizers from waste woods of artificial bed log for shiitake* shiitake aseptic timber and other edible or medicinal fungi culture base

1977
- 1977-06-03 DE DE19772725146 patent/DE2725146A1/de not_active Withdrawn
1978
- 1978-05-24 IL IL54779A patent/IL54779A/xx unknown
- 1978-05-26 PT PT197868091A patent/PT68091A/pt unknown
- 1978-05-29 IE IE1065/78A patent/IE46905B1/en unknown
- 1978-05-29 AU AU36576/78A patent/AU519196B2/en not_active Expired
- 1978-05-29 CA CA304,279A patent/CA1110264A/en not_active Expired
- 1978-05-30 TR TR20048A patent/TR20048A/xx unknown
- 1978-05-31 ES ES470367A patent/ES470367A1/es not_active Expired
- 1978-06-01 DD DD78205730A patent/DD135853A5/xx unknown
- 1978-06-01 DE DE7878100050T patent/DE2860287D1/de not_active Expired
- 1978-06-01 EP EP78100050A patent/EP0000030B1/de not_active Expired
- 1978-06-01 CS CS783577A patent/CS196429B2/cs unknown
- 1978-06-01 PL PL1978207278A patent/PL106564B1/xx unknown
- 1978-06-01 SU SU782619253A patent/SU725541A3/ru active
- 1978-06-01 BR BR787803528A patent/BR7803528A/pt unknown
- 1978-06-02 YU YU01325/78A patent/YU132578A/xx unknown
- 1978-06-02 NO NO781931A patent/NO781931L/no unknown
- 1978-06-02 IT IT49686/78A patent/IT1104710B/it active
- 1978-06-02 AT AT403178A patent/AT358869B/de not_active IP Right Cessation
- 1978-06-02 HU HU78BA3662A patent/HU177551B/hu unknown
- 1978-06-02 ZA ZA00783163A patent/ZA783163B/xx unknown
- 1978-06-02 DK DK247278A patent/DK247278A/da not_active Application Discontinuation
- 1978-06-02 FI FI781762A patent/FI781762A/fi not_active Application Discontinuation
- 1978-06-02 NZ NZ187460A patent/NZ187460A/xx unknown
- 1978-06-02 JP JP6587678A patent/JPS543038A/ja active Granted

Also Published As

Publication number	Publication date
ES470367A1 (es)	1979-09-16
EP0000030B1 (de)	1980-12-10
DK247278A (da)	1978-12-04
YU132578A (en)	1983-01-21
PL207278A1 (pl)	1979-03-26
DE2725146A1 (de)	1978-12-14
IL54779A (en)	1982-12-31
AU519196B2 (en)	1981-11-19
JPS543038A (en)	1979-01-11
ATA403178A (de)	1980-02-15
DE2860287D1 (en)	1981-02-19
IE46905B1 (en)	1983-11-02
CA1110264A (en)	1981-10-06
PT68091A (fr)	1978-05-31
IE781065L (en)	1978-12-03
FI781762A (fi)	1978-12-04
ZA783163B (en)	1979-07-25
SU725541A1 (ru)	1980-03-30
EP0000030A1 (de)	1978-12-20
PL106564B1 (pl)	1979-12-31
BR7803528A (pt)	1979-02-20
SU725541A3 (en)	1980-03-30
IT7849686A0 (it)	1978-06-02
NZ187460A (en)	1980-11-28
NO781931L (no)	1978-12-05
TR20048A (tr)	1980-07-02
JPS6151583B2 (da)	1986-11-10
DD135853A5 (de)	1979-06-06
IL54779A0 (en)	1978-07-31
AU3657678A (en)	1979-12-06
AT358869B (de)	1980-10-10
HU177551B (en)	1981-11-28
IT1104710B (it)	1985-10-28

Publication	Publication Date	Title
JP2753872B2 (ja)	1998-05-20	スルファモイルフェニル尿素
DE4038430A1 (de)	1992-06-04	Herbizide n-((1,3,5-triazin-2-yl)-aminocarbonyl) benzolsulfonamide
ITMI970554A1 (it)	1998-09-13	Amminosolfoniluree ad attivita' erbicida
CS207776B2 (en)	1981-08-31	Herbicide means
US5139565A (en)	1992-08-18	Substituted pyridinesulfonamide compounds, and herbicidal compositions containing them
CS277621B6 (en)	1993-03-17	Herbicidally active ester of /\|(1,3,5-triazin-2-yl)aminocarbonyl¨aminosulfonyl/benzoic acid, process of its preparation and use
CS196228B2 (en)	1980-03-31	Herbicide
US4500340A (en)	1985-02-19	Urea derivatives and their use for controlling undesirable plant growth
DE4238175A1 (de)	1994-05-19	Herbizide Sulfonylharnstoffe, Verfahren zur Herstellung und ihre Verwendung
DE4206146A1 (de)	1993-09-02	Herbizide n-((1,3,5-triazin-2-yl)aminocarbonyl)benzolsulfonamide
DE3882290T2 (de)	1993-10-28	2-(Substituierte imino)-1,3,4-Dihydrothiadiazole.
CS196429B2 (en)	1980-03-31	Herbicide
HU189217B (en)	1986-06-30	Herbicide compositions containing 4,5-dimethoxy-pyridazone derivatives and process for producing the active agents
US3962306A (en)	1976-06-08	Sulfonyloxyphenylurea compounds and herbicidal compositions
CA1120942A (en)	1982-03-30	.sup.m-anilide-urethanes
US4344790A (en)	1982-08-17	Carbaminic acid esters with herbicidal properties
HU185912B (en)	1985-04-28	Herbicide compositions containing 6h-1,2,4,6-triatriazine-1,1-dioxide derivatives and process for preparing the active substances
CS242883B2 (en)	1986-05-15	Herbicide and method of its efficient component production
HU190948B (en)	1986-12-28	Herbicide compositions containing n-acyl-anthranilic acid derivatives as active agents and process for producing the active agents
CS210629B2 (en)	1982-01-29	Herbicide
FI62059C (fi)	1982-11-10	Herbicidala (3-(n'-(halogenfluorfenyl)-karbamoyloxi)-fenyl)-karbamater
CS208667B2 (en)	1981-09-15	Herbicide means and method of making the active substances
PL106526B1 (pl)	1979-12-31	Srodek chwastobojczy
CS236785B2 (en)	1985-05-15	Herbicide agent and processing method of active components
EP0123727B1 (de)	1986-08-20	Substituierte Harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses