DD151863A5 - Schaedlingsbekaempfungsmittel - Google Patents

Schaedlingsbekaempfungsmittel Download PDF

Info

Publication number: DD151863A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; dimethyl; carbamic acid; pyrimidinyl; formula
Prior art date: 1979-07-12

Application number

DD80222539A

Other languages

German (de)

English (en)

Inventor

Fritz Maurer

Ingeborg Hammann

Bernhard Homeyer

Original Assignee

Bayer 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.)

1979-07-12

Filing date

1980-07-10

Publication date

1981-11-11

1980-07-10 Application filed by Bayer Ag filed Critical Bayer Ag

1981-11-11 Publication of DD151863A5 publication Critical patent/DD151863A5/de

Links

229910052757 nitrogen Inorganic materials 0.000 claims abstract description 24
239000004480 active ingredient Substances 0.000 claims abstract description 12
239000004606 Fillers/Extenders Substances 0.000 claims abstract description 4
239000004094 surface-active agent Substances 0.000 claims abstract description 4
238000000034 method Methods 0.000 claims description 23
238000002360 preparation method Methods 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 9
241000607479 Yersinia pestis Species 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 7
150000002148 esters Chemical class 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000004414 alkyl thio group Chemical group 0.000 claims description 5
239000000575 pesticide Substances 0.000 claims description 5
125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 4
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
238000002156 mixing Methods 0.000 claims description 2
RJZWXBPGTVPSRE-UHFFFAOYSA-N pyrimidin-2-yl carbamate Chemical compound NC(=O)OC1=NC=CC=N1 RJZWXBPGTVPSRE-UHFFFAOYSA-N 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract description 27
239000000203 mixture Substances 0.000 abstract description 20
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BPCFBUOIUJCLTD-UHFFFAOYSA-N pyrimidin-2-yl N,N-dimethoxycarbamate Chemical compound CON(C(OC1=NC=CC=N1)=O)OC BPCFBUOIUJCLTD-UHFFFAOYSA-N 0.000 abstract description 7
UCERVHYBSTYCQS-UHFFFAOYSA-N 4-methyl-2-methylsulfanylpyrimidine Chemical compound CSC1=NC=CC(C)=N1 UCERVHYBSTYCQS-UHFFFAOYSA-N 0.000 abstract description 5
229940112021 centrally acting muscle relaxants carbamic acid ester Drugs 0.000 abstract description 2
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-1 5-substituted 2-chloromethyl-6-hydroxypyrimidines Chemical class 0.000 description 18
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HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
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PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
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XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
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WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
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229910052750 molybdenum Inorganic materials 0.000 description 1
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IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
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JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
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229920002689 polyvinyl acetate Polymers 0.000 description 1
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TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
239000002243 precursor Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
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FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
125000004943 pyrimidin-6-yl group Chemical group N1=CN=CC=C1* 0.000 description 1
239000010453 quartz Substances 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
238000001953 recrystallisation Methods 0.000 description 1
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150000003839 salts Chemical class 0.000 description 1
239000000523 sample Substances 0.000 description 1
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150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000779 smoke Substances 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
241000894007 species Species 0.000 description 1
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YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
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239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/56—One oxygen atom and one sulfur atom
- 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
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
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)

DD80222539A 1979-07-12 1980-07-10 Schaedlingsbekaempfungsmittel DD151863A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19792928185 DE2928185A1 (de)	1979-07-12	1979-07-12	N,n-dimethyl-o-pyrimidinyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel

Publications (1)

Publication Number	Publication Date
DD151863A5 true DD151863A5 (de)	1981-11-11

Family

ID=6075551

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD80222539A DD151863A5 (de)	1979-07-12	1980-07-10	Schaedlingsbekaempfungsmittel

Country Status (21)

Country	Link
US (1)	US4323571A (es)
EP (1)	EP0022511B1 (es)
JP (1)	JPS5615274A (es)
AR (1)	AR226311A1 (es)
AT (1)	ATE2744T1 (es)
AU (1)	AU531828B2 (es)
BR (1)	BR8004335A (es)
CA (1)	CA1140131A (es)
DD (1)	DD151863A5 (es)
DE (2)	DE2928185A1 (es)
DK (1)	DK301580A (es)
EG (1)	EG14420A (es)
ES (1)	ES493329A0 (es)
GR (1)	GR69302B (es)
HU (1)	HU185220B (es)
IL (1)	IL60534A (es)
NZ (1)	NZ194281A (es)
PH (1)	PH17632A (es)
PT (1)	PT71484A (es)
TR (1)	TR20743A (es)
ZA (1)	ZA804179B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3211035A1 (de) *	1982-03-25	1983-09-29	Bayer Ag, 5090 Leverkusen	Substituierte n,n-dimethyl-o-pyrimidin-e-yl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
DE3247926A1 (de) *	1982-12-24	1984-06-28	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von 2-alkylthiomethyl-4-hydroxypyrimidinen
US4521811A (en) *	1984-05-02	1985-06-04	Rca Corporation	Beam current limiting arrangement for a digital television system
DE3436478A1 (de) *	1984-10-05	1986-04-17	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von n,n-dimethyl-0-pyrimidinylcarbaminsaeureester
DE3444494A1 (de) *	1984-12-06	1986-06-19	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von alkylthioacetamidinen
EP0218171A3 (de) *	1985-10-09	1988-01-13	Bayer Ag	Verfahren zur Herstellung von 2-Alkylsulfonylalkylen-pyrimidinen
DE3911488A1 (de) *	1989-04-08	1990-10-11	Bayer Ag	Pyrimidin-4-yl-carbamidsaeureester

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH281966A (de) *	1949-08-22	1952-03-31	Ag J R Geigy	Verfahren zur Herstellung eines heterocyclischen Carbaminsäurederivates.
FR1443910A (fr)	1965-01-25	1966-07-01	Bombrini Parodi Delfino S P A	Compositions destinées à la lutte contre les insectes qui résistent aux insecticides chlorés
DE2752613A1 (de) *	1977-11-25	1979-06-07	Bayer Ag	N,n-dialkyl-0-pyrimidinyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide
GR73662B (es) *	1978-07-07	1984-03-28	Ciba Geigy Ag
DE2838359A1 (de) *	1978-09-02	1980-03-20	Bayer Ag	N,n-dimethyl-0-pyrimidinyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel

1979
- 1979-07-12 DE DE19792928185 patent/DE2928185A1/de not_active Withdrawn
1980
- 1980-06-20 US US06/161,540 patent/US4323571A/en not_active Expired - Lifetime
- 1980-07-01 DE DE8080103720T patent/DE3062274D1/de not_active Expired
- 1980-07-01 AT AT80103720T patent/ATE2744T1/de not_active IP Right Cessation
- 1980-07-01 EP EP80103720A patent/EP0022511B1/de not_active Expired
- 1980-07-02 PT PT71484A patent/PT71484A/pt unknown
- 1980-07-09 TR TR20743A patent/TR20743A/xx unknown
- 1980-07-09 NZ NZ194281A patent/NZ194281A/xx unknown
- 1980-07-09 IL IL60534A patent/IL60534A/xx unknown
- 1980-07-10 DD DD80222539A patent/DD151863A5/de unknown
- 1980-07-10 GR GR62425A patent/GR69302B/el unknown
- 1980-07-10 JP JP9333980A patent/JPS5615274A/ja active Granted
- 1980-07-10 CA CA000355906A patent/CA1140131A/en not_active Expired
- 1980-07-11 BR BR8004335A patent/BR8004335A/pt unknown
- 1980-07-11 AR AR281745A patent/AR226311A1/es active
- 1980-07-11 ZA ZA00804179A patent/ZA804179B/xx unknown
- 1980-07-11 AU AU60333/80A patent/AU531828B2/en not_active Ceased
- 1980-07-11 ES ES493329A patent/ES493329A0/es active Granted
- 1980-07-11 DK DK301580A patent/DK301580A/da not_active Application Discontinuation
- 1980-07-11 HU HU801743A patent/HU185220B/hu unknown
- 1980-07-12 EG EG411/80A patent/EG14420A/xx active
- 1980-07-14 PH PH24288A patent/PH17632A/en unknown

Also Published As

Publication number	Publication date
IL60534A0 (en)	1980-09-16
DK301580A (da)	1981-01-13
IL60534A (en)	1986-02-28
ES8105984A1 (es)	1981-07-01
JPS5615274A (en)	1981-02-14
NZ194281A (en)	1982-03-09
PH17632A (en)	1984-10-12
EP0022511B1 (de)	1983-03-09
HU185220B (en)	1984-12-28
DE3062274D1 (en)	1983-04-14
BR8004335A (pt)	1981-01-27
AU531828B2 (en)	1983-09-08
ATE2744T1 (de)	1983-03-15
CA1140131A (en)	1983-01-25
AU6033380A (en)	1981-01-15
US4323571A (en)	1982-04-06
JPH03389B2 (es)	1991-01-07
EP0022511A2 (de)	1981-01-21
EG14420A (en)	1984-03-31
ZA804179B (en)	1981-08-26
GR69302B (es)	1982-05-14
PT71484A (en)	1980-08-01
DE2928185A1 (de)	1981-01-29
TR20743A (tr)	1982-06-24
EP0022511A3 (en)	1981-04-15
ES493329A0 (es)	1981-07-01
AR226311A1 (es)	1982-06-30

Publication	Publication Date	Title
EP0315826A1 (de)	1989-05-17	Imidazoline
EP0000887B1 (de)	1980-10-29	Cyclopropylsubstituierte Pyrimidin(4)yl(thiono)-(thiol)-phosphor(phosphon)-säureester bzw. -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide
DE2839270A1 (de)	1980-03-20	N,n-dimethyl-o-pyrazolyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
EP0022511B1 (de)	1983-03-09	N,N-Dimethyl-O-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Schädlingsbekämpfungsmittel
EP0017066B1 (de)	1982-04-28	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0008762B1 (de)	1981-10-21	N,N-Dimethyl-O-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0002200B1 (de)	1981-09-02	N,N-Dialkyl-O-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0000198B1 (de)	1980-07-23	N,N-Dialkyl-0-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0005240B1 (de)	1981-04-29	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0009103B1 (de)	1981-04-29	N-(O-Äthyl-S-n-propyl-(di)thiophosphoryloxy)-naphtalimide, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Schädlingsbekämpfungsmittel, ihre Herstellung und Verwendung
DE2831165A1 (de)	1980-01-24	2-cyclopropyl-pyrimidin(4)yl-thionophosphonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0090247B1 (de)	1986-07-23	Substituierte N,N-Dimethyl-O-pyrimidin-4-yl-carbamin-säureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0000388B1 (de)	1980-11-26	Pyridazinon(thiono)-phosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide
DE3003019A1 (de)	1981-07-30	N,n-dimethyl-o-(4,6-dihydro-2h-thieno (3,4-c) pyrazol-3-yl)-carbaminsaeure-ester sowie deren 5-oxide und 5,5-dioxide, verfahren zu deren herstellung und ihre verwendung in schaedlingsbekaempfungsmitteln
DE3114833A1 (de)	1982-11-04	N-alkyl-0-pyrazol-4-yl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
EP0087561B1 (de)	1986-01-29	N,N-Dimethyl-0-(1-carbamoyl-5-pyrazolyl)-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
DE2639256A1 (de)	1978-03-02	Alkoxy- bzw. alkylthiosubstituierte pyrimidin(thiono)-(thiol)-phosphor(phosphon)-saeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0000895A1 (de)	1979-03-07	Aryl-N-alkyl-carbamate, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
DE3438919A1 (de)	1986-04-24	Substituierte phenyl-carbaminsaeureester
DE3426007A1 (de)	1986-01-16	Pyrimidinyl-thionophosphorsaeureester
EP0075144A1 (de)	1983-03-30	N,N-Dimethyl-O-imidazol-4-yl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
DE2637007A1 (de)	1978-02-23	Isoxazolyl(thiono) (thiol)-phosphor (phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide
DE3716299A1 (de)	1988-11-24	Thionophosphorsaeureester