NZ196541A - 2-haloacentanilides and herbicidal compositions - Google Patents

2-haloacentanilides and herbicidal compositions

Info

Publication number: NZ196541A
Authority: NZ; New Zealand
Prior art keywords: compound; chloroacetanilide; methyl; ethyl; trifluoromethyl
Prior art date: 1980-03-25

Application number

NZ196541A

Other languages

English (en)

Inventor

J P Chupp

Original Assignee

Monsanto Co

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.)

1980-03-25

Filing date

1981-03-18

Publication date

1984-04-27

1981-03-18 Application filed by Monsanto Co filed Critical Monsanto Co

1984-04-27 Publication of NZ196541A publication Critical patent/NZ196541A/en

Links

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238000000034 method Methods 0.000 claims description 42
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125000000217 alkyl group Chemical group 0.000 claims description 9
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206010015946 Eye irritation Diseases 0.000 description 1
WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical compound F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 description 1
244000248416 Fagopyrum cymosum Species 0.000 description 1
241000209082 Lolium Species 0.000 description 1
241000146051 Malvella leprosa Species 0.000 description 1
RRVIAQKBTUQODI-UHFFFAOYSA-N Methabenzthiazuron Chemical compound C1=CC=C2SC(N(C)C(=O)NC)=NC2=C1 RRVIAQKBTUQODI-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
241001148659 Panicum dichotomiflorum Species 0.000 description 1
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235000003675 Paspalum scrobiculatum Nutrition 0.000 description 1
240000004928 Paspalum scrobiculatum Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
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ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
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ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
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239000003849 aromatic solvent Substances 0.000 description 1
METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
150000001559 benzoic acids Chemical class 0.000 description 1
CHQVQXZFZHACQQ-UHFFFAOYSA-M benzyl(triethyl)azanium;bromide Chemical compound [Br-].CC[N+](CC)(CC)CC1=CC=CC=C1 CHQVQXZFZHACQQ-UHFFFAOYSA-M 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
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YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
239000002775 capsule Substances 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
OIQPTROHQCGFEF-UHFFFAOYSA-L chembl1371409 Chemical compound [Na+].[Na+].OC1=CC=C2C=C(S([O-])(=O)=O)C=CC2=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 OIQPTROHQCGFEF-UHFFFAOYSA-L 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
FCYRSDMGOLYDHL-UHFFFAOYSA-N chloromethoxyethane Chemical compound CCOCCl FCYRSDMGOLYDHL-UHFFFAOYSA-N 0.000 description 1
229940125807 compound 37 Drugs 0.000 description 1
235000009508 confectionery Nutrition 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000001186 cumulative effect Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
229940116901 diethyldithiocarbamate Drugs 0.000 description 1
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238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical compound Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 description 1
231100000013 eye irritation Toxicity 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
239000003815 herbicide antidote Substances 0.000 description 1
238000004128 high performance liquid chromatography Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000005457 ice water Substances 0.000 description 1
229910052900 illite Inorganic materials 0.000 description 1
238000010952 in-situ formation Methods 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000009533 lab test Methods 0.000 description 1
XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
159000000003 magnesium salts Chemical class 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
WMIPWRSVIZFVQB-UHFFFAOYSA-N n,n-dimethyl-2,2-diphenylacetamide Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1.C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 WMIPWRSVIZFVQB-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
JXTHEWSKYLZVJC-UHFFFAOYSA-N naptalam Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC2=CC=CC=C12 JXTHEWSKYLZVJC-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
239000008188 pellet Substances 0.000 description 1
230000002688 persistence Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Chemical class 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
239000003444 phase transfer catalyst Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
230000008654 plant damage Effects 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000056 polyoxyethylene ether Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229940072033 potash Drugs 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000009877 rendering Methods 0.000 description 1
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
229940043267 rhodamine b Drugs 0.000 description 1
231100000817 safety factor Toxicity 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
230000036556 skin irritation Effects 0.000 description 1
231100000475 skin irritation Toxicity 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
AUPJTDWZPFFCCP-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCCN(C)CCS([O-])(=O)=O AUPJTDWZPFFCCP-GMFCBQQYSA-M 0.000 description 1
HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229940104261 taurate Drugs 0.000 description 1
238000010998 test method Methods 0.000 description 1
231100000041 toxicology testing Toxicity 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Medicines Containing Plant Substances (AREA)

NZ196541A 1980-03-25 1981-03-18 2-haloacentanilides and herbicidal compositions NZ196541A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US13371880A	1980-03-25	1980-03-25

Publications (1)

Publication Number	Publication Date
NZ196541A true NZ196541A (en)	1984-04-27

Family

ID=22459986

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NZ196541A NZ196541A (en)	1980-03-25	1981-03-18	2-haloacentanilides and herbicidal compositions

Country Status (40)

Country	Link
JP (1)	JPS56145260A (sv)
AR (1)	AR228451A1 (sv)
AT (1)	AT370279B (sv)
AU (1)	AU537092B2 (sv)
BE (1)	BE887997A (sv)
BG (1)	BG36192A3 (sv)
BR (1)	BR8101599A (sv)
CA (1)	CA1221380A (sv)
CH (1)	CH644586A5 (sv)
CS (1)	CS227326B2 (sv)
CY (1)	CY1278A (sv)
DD (1)	DD157295A5 (sv)
DE (1)	DE3110523C2 (sv)
DK (1)	DK157189C (sv)
EG (1)	EG15025A (sv)
FI (1)	FI73972C (sv)
FR (1)	FR2479204B1 (sv)
GB (1)	GB2072181B (sv)
GR (1)	GR66543B (sv)
HU (1)	HU189497B (sv)
IE (1)	IE51698B1 (sv)
IL (2)	IL62411A (sv)
IT (1)	IT1194040B (sv)
KE (1)	KE3480A (sv)
LU (1)	LU83232A1 (sv)
MA (1)	MA19103A1 (sv)
MW (1)	MW1181A1 (sv)
MX (1)	MX6765E (sv)
NL (1)	NL8101326A (sv)
NO (1)	NO151617C (sv)
NZ (1)	NZ196541A (sv)
OA (1)	OA06771A (sv)
PL (1)	PL125386B1 (sv)
PT (1)	PT72685B (sv)
RO (3)	RO85642B (sv)
SE (1)	SE462093B (sv)
SG (1)	SG86784G (sv)
TR (1)	TR20869A (sv)
ZA (2)	ZA811808B (sv)
ZW (1)	ZW6081A1 (sv)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0192628A1 (en) *	1985-02-13	1986-08-27	Monsanto Company	Novel acetanilides and their use in the regulation of the natural growth or development of turf grass

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH585191A5 (en) *	1973-02-08	1977-02-28	Ciba Geigy Ag	N-substd halogen acetanilide herbicides - prepd. from N-substd anilines and chloracetic anhydride or chloracetyl chloride
CH579348A5 (sv) *	1973-02-08	1976-09-15	Ciba Geigy Ag
PL103793B1 (pl) *	1976-03-19	1979-07-31	Monsanto Co	Srodek chwastobojczy
DE2803662A1 (de) *	1978-01-25	1979-07-26	Schering Ag	Chloracetanilide, verfahren zur herstellung dieser verbindungen sowie diese enthaltende herbizide mittel
US4258196A (en) *	1978-04-17	1981-03-24	Monsanto Company	Process for the production of tertiary 2-haloacetamides

1981
- 1981-03-18 AU AU68490/81A patent/AU537092B2/en not_active Ceased
- 1981-03-18 NZ NZ196541A patent/NZ196541A/en unknown
- 1981-03-18 NO NO810927A patent/NO151617C/no unknown
- 1981-03-18 BE BE0/204164A patent/BE887997A/fr not_active IP Right Cessation
- 1981-03-18 MX MX819355U patent/MX6765E/es unknown
- 1981-03-18 BG BG051267A patent/BG36192A3/xx unknown
- 1981-03-18 AT AT0125681A patent/AT370279B/de not_active IP Right Cessation
- 1981-03-18 MW MW11/81A patent/MW1181A1/xx unknown
- 1981-03-18 CA CA000373332A patent/CA1221380A/en not_active Expired
- 1981-03-18 TR TR20869A patent/TR20869A/xx unknown
- 1981-03-18 DE DE3110523A patent/DE3110523C2/de not_active Expired
- 1981-03-18 IE IE596/81A patent/IE51698B1/en unknown
- 1981-03-18 IT IT20413/81A patent/IT1194040B/it active
- 1981-03-18 GB GB8108383A patent/GB2072181B/en not_active Expired
- 1981-03-18 JP JP3808481A patent/JPS56145260A/ja active Granted
- 1981-03-18 MA MA19309A patent/MA19103A1/fr unknown
- 1981-03-18 SE SE8101736A patent/SE462093B/sv not_active IP Right Cessation
- 1981-03-18 GR GR64439A patent/GR66543B/el unknown
- 1981-03-18 DD DD81228415A patent/DD157295A5/de not_active IP Right Cessation
- 1981-03-18 PT PT72685A patent/PT72685B/pt unknown
- 1981-03-18 CS CS811984A patent/CS227326B2/cs unknown
- 1981-03-18 RO RO110027A patent/RO85642B/ro unknown
- 1981-03-18 BR BR8101599A patent/BR8101599A/pt unknown
- 1981-03-18 NL NL8101326A patent/NL8101326A/nl not_active Application Discontinuation
- 1981-03-18 HU HU81693A patent/HU189497B/hu not_active IP Right Cessation
- 1981-03-18 LU LU83232A patent/LU83232A1/fr unknown
- 1981-03-18 IL IL62411A patent/IL62411A/xx unknown
- 1981-03-18 EG EG144/81A patent/EG15025A/xx active
- 1981-03-18 RO RO81103729A patent/RO81727A/ro unknown
- 1981-03-18 FR FR8105442A patent/FR2479204B1/fr not_active Expired
- 1981-03-18 ZA ZA00811808A patent/ZA811808B/xx unknown
- 1981-03-18 OA OA57357A patent/OA06771A/xx unknown
- 1981-03-18 CH CH185581A patent/CH644586A5/de not_active IP Right Cessation
- 1981-03-18 DK DK120681A patent/DK157189C/da active
- 1981-03-18 CY CY1278A patent/CY1278A/en unknown
- 1981-03-18 IL IL62420A patent/IL62420A/xx unknown
- 1981-03-18 AR AR284653A patent/AR228451A1/es active
- 1981-03-18 ZA ZA828914A patent/ZA828914B/xx unknown
- 1981-03-18 RO RO110026A patent/RO85641B/ro unknown
- 1981-03-18 FI FI810834A patent/FI73972C/sv not_active IP Right Cessation
- 1981-03-18 ZW ZW60/81A patent/ZW6081A1/xx unknown
- 1981-03-18 PL PL1981230198A patent/PL125386B1/pl unknown
1984
- 1984-11-29 KE KE3480A patent/KE3480A/xx unknown
- 1984-12-04 SG SG867/84A patent/SG86784G/en unknown

Also Published As

Publication number	Publication date
IT8120413A0 (it)	1981-03-18
FI73972C (sv)	1987-12-10
IE810596L (en)	1981-09-25
ZW6081A1 (en)	1981-08-05
GB2072181A (en)	1981-09-30
SE462093B (sv)	1990-05-07
HU189497B (en)	1986-07-28
DK157189B (da)	1989-11-20
BR8101599A (pt)	1981-09-29
NO810927L (no)	1981-09-28
SG86784G (en)	1985-06-07
AR228451A1 (es)	1983-03-15
ZA811808B (en)	1983-02-23
EG15025A (en)	1985-12-31
DD157295A5 (de)	1982-11-03
DE3110523C2 (de)	1986-02-06
IL62420A0 (en)	1981-05-20
GR66543B (sv)	1981-03-26
DK157189C (da)	1990-04-23
RO85642B (ro)	1984-11-30
GB2072181B (en)	1984-02-29
RO81727B (ro)	1983-05-30
CA1221380A (en)	1987-05-05
KE3480A (en)	1985-01-04
RO85642A (ro)	1984-11-25
RO81727A (ro)	1983-06-01
AU537092B2 (en)	1984-06-07
CY1278A (en)	1985-07-05
AU6849081A (en)	1981-10-01
ATA125681A (de)	1982-08-15
MW1181A1 (en)	1983-02-09
FI810834L (fi)	1981-09-26
PT72685A (en)	1981-04-01
PL230198A1 (sv)	1981-10-30
MX6765E (es)	1986-06-27
CH644586A5 (de)	1984-08-15
FR2479204A1 (fr)	1981-10-02
PT72685B (en)	1982-03-24
IE51698B1 (en)	1987-02-18
NO151617B (no)	1985-01-28
IT1194040B (it)	1988-08-31
IL62420A (en)	1985-06-30
IL62411A0 (en)	1981-05-20
IL62411A (en)	1984-07-31
LU83232A1 (fr)	1981-10-30
FI73972B (fi)	1987-08-31
RO85641A (ro)	1984-11-25
BG36192A3 (en)	1984-09-14
CS227326B2 (en)	1984-04-16
NO151617C (no)	1985-05-08
JPH0148260B2 (sv)	1989-10-18
MA19103A1 (fr)	1981-10-01
DK120681A (da)	1981-09-26
BE887997A (fr)	1981-09-18
ZA828914B (en)	1983-02-23
OA06771A (fr)	1982-06-30
DE3110523A1 (de)	1982-01-14
SE8101736L (sv)	1981-11-09
TR20869A (tr)	1982-11-18
JPS56145260A (en)	1981-11-11
PL125386B1 (en)	1983-05-31
AT370279B (de)	1983-03-10
NL8101326A (nl)	1981-10-16
RO85641B (ro)	1984-11-30
FR2479204B1 (fr)	1985-08-16

Publication	Publication Date	Title
EP0205271B1 (en)	1989-02-01	N-(3-chloro-4-isopropylphenyl)carboxamides, process for producing them, and selective herbicides containing them
US4345938A (en)	1982-08-24	Herbicidal 2-haloacetanilides
US3140167A (en)	1964-07-07	2, 6-di-t-butyl-4-substituted phenyl nu-methyl carbamate and use thereof as selective herbicides
US3869513A (en)	1975-03-04	Dinitro-dialklyamino-acetophenones
NZ196541A (en)	1984-04-27	2-haloacentanilides and herbicidal compositions
US4761176A (en)	1988-08-02	Herbicidal 2-haloacetanilides
US4605764A (en)	1986-08-12	Substituted acetamide derivatives with an antidote action, antidote compositions containing such compounds, selective herbicide compositions containing these antidotes and a process for the preparation of substituted acetamide derivatives
US4758263A (en)	1988-07-19	2-(2,5-difluorophenyl)-4-methyl-1,2,4-oxadiazolidine-3,5 diones
US4567299A (en)	1986-01-28	Herbicidal 2-haloacetanilides
US4731109A (en)	1988-03-15	Herbicidal 2-haloacetanilides
US4606759A (en)	1986-08-19	Herbicidal 2-haloacetanilides
CA1221379A (en)	1987-05-05	Herbicidal 2-haloacetanilides
CA1221378A (en)	1987-05-05	Herbicidal 2-haloacetanilides
DD156664A5 (de)	1982-09-15	Herbizide und den pflanzenwuchs hemmende mittel
PL89203B1 (en)	1976-11-30	2-Chloro-N-(2'-methoxypropyl)- and 2-chloro-N-(2'-ethoxypropyl)-2'',6''-dimethyl-acetanilide as long term weed killers[US4412855A]
GB2072177A (en)	1981-09-30	Herbicidal 2-Haloacetanilides
US4155747A (en)	1979-05-22	Derivatives of tetrahydro-1,3,5-oxadiazin-4-one and herbicidal compositions containing these derivatives
CA1206165A (en)	1986-06-17	Herbicidal 2-haloacetanilides
US3445222A (en)	1969-05-20	Herbicidal compositions containing trisubstituted-phenyl n-methylcarbamates
NZ196549A (en)	1984-02-03	2-haloacetanilides and herbicidal compositions
NZ206253A (en)	1986-04-11	N,n-dialkyl-2-(4-substituted-alpha-naphthoxy)-propion-amides and herbicidal compositions
DD149892A5 (de)	1981-08-05	Herbizides mittel