NL8320114A - Plantenbeschermingsmiddel. - Google Patents

Plantenbeschermingsmiddel. Download PDF

Info

Publication number: NL8320114A
Authority: NL; Netherlands
Prior art keywords: und; cycloalkyl; die; oder; saturated
Prior art date: 1982-04-20

Application number

NL8320114A

Other languages

English (en)

Dutch (nl)

Original Assignee

Borsodi Vegyi Komb

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.)

1982-04-20

Filing date

1983-04-20

Publication date

1984-03-01

1983-04-20 Application filed by Borsodi Vegyi Komb filed Critical Borsodi Vegyi Komb

1984-03-01 Publication of NL8320114A publication Critical patent/NL8320114A/nl

Links

230000001681 protective effect Effects 0.000 title 1
-1 alkoxycarbonyl dithiocarbamates Chemical class 0.000 claims description 33
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 19
125000000753 cycloalkyl group Chemical group 0.000 claims description 13
229920006395 saturated elastomer Polymers 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 12
125000004417 unsaturated alkyl group Chemical group 0.000 claims description 11
239000011814 protection agent Substances 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 7
125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
238000002360 preparation method Methods 0.000 claims description 7
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 6
125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
125000004430 oxygen atom Chemical group O* 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
229910052717 sulfur Inorganic materials 0.000 claims description 6
125000004434 sulfur atom Chemical group 0.000 claims description 6
239000013543 active substance Substances 0.000 claims description 5
239000003085 diluting agent Substances 0.000 claims description 5
239000007788 liquid Substances 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
239000012990 dithiocarbamate Substances 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
239000012736 aqueous medium Substances 0.000 claims description 2
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims 3
150000004945 aromatic hydrocarbons Chemical class 0.000 claims 2
150000008280 chlorinated hydrocarbons Chemical class 0.000 claims 2
239000000460 chlorine Substances 0.000 claims 2
239000004615 ingredient Substances 0.000 claims 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
241000195493 Cryptophyta Species 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
150000001412 amines Chemical group 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
229910052801 chlorine Inorganic materials 0.000 claims 1
238000010413 gardening Methods 0.000 claims 1
239000000463 material Substances 0.000 claims 1
239000002609 medium Substances 0.000 claims 1
150000003560 thiocarbamic acids Chemical class 0.000 claims 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 10
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
239000001963 growth medium Substances 0.000 description 8
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 8
241000196324 Embryophyta Species 0.000 description 7
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
241000607479 Yersinia pestis Species 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
239000004476 plant protection product Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
230000002538 fungal effect Effects 0.000 description 3
239000000417 fungicide Substances 0.000 description 3
239000000203 mixture Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241001465180 Botrytis Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
241000223195 Fusarium graminearum Species 0.000 description 2
241000233622 Phytophthora infestans Species 0.000 description 2
241000228452 Venturia inaequalis Species 0.000 description 2
150000004659 dithiocarbamates Chemical class 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000003350 kerosene Substances 0.000 description 2
IVRIRQXJSNCSPQ-UHFFFAOYSA-N propan-2-yl carbonochloridate Chemical compound CC(C)OC(Cl)=O IVRIRQXJSNCSPQ-UHFFFAOYSA-N 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000012360 testing method Methods 0.000 description 2
229920001817 Agar Polymers 0.000 description 1
238000012935 Averaging Methods 0.000 description 1
235000021537 Beetroot Nutrition 0.000 description 1
YVUIGFPNYBVWGI-UHFFFAOYSA-N CCCC(C)(C)OC([SH2]C(N(NC)NC)=S)=O Chemical compound CCCC(C)(C)OC([SH2]C(N(NC)NC)=S)=O YVUIGFPNYBVWGI-UHFFFAOYSA-N 0.000 description 1
BGCIDSMEJKXXOM-UHFFFAOYSA-N CCN(CC)C([SH2]C(OC(C)C)=O)=S Chemical compound CCN(CC)C([SH2]C(OC(C)C)=O)=S BGCIDSMEJKXXOM-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
241000206672 Gelidium Species 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
235000010419 agar Nutrition 0.000 description 1
238000012271 agricultural production Methods 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000013078 crystal Substances 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
PFNYKXQYOYYJAU-UHFFFAOYSA-N diethylcarbamodithioic acid;sodium Chemical compound [Na].CCN(CC)C(S)=S PFNYKXQYOYYJAU-UHFFFAOYSA-N 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
238000004362 fungal culture Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
239000002054 inoculum Substances 0.000 description 1
238000009630 liquid culture Methods 0.000 description 1
231100000989 no adverse effect Toxicity 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
238000003976 plant breeding Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
VNMLVHLVBFHHSN-UHFFFAOYSA-N thiophen-2-ylcarbamic acid Chemical class OC(=O)NC1=CC=CS1 VNMLVHLVBFHHSN-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 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
- 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
- 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
- A01N47/12—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, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- 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
- A01N47/12—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, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues 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
- A01N47/20—N-Aryl derivatives 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)

NL8320114A 1982-04-20 1983-04-20 Plantenbeschermingsmiddel. NL8320114A (nl)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
HU120582		1982-04-20
HU821205A HU187452B (en)	1982-04-20	1982-04-20	Fungicides containing - as reagent - alkoxicarbonile ditiocarbamata and process for production of the reagent
HU8300017		1983-04-20
PCT/HU1983/000017 WO1983003603A1 (fr)	1982-04-20	1983-04-20	Agent protecteur de plantes

Publications (1)

Publication Number	Publication Date
NL8320114A true NL8320114A (nl)	1984-03-01

Family

ID=10953330

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8320114A NL8320114A (nl)	1982-04-20	1983-04-20	Plantenbeschermingsmiddel.

Country Status (12)

Country	Link
US (1)	US4613615A (fr)
JP (1)	JPS59500766A (fr)
AT (1)	AT386927B (fr)
CH (1)	CH660482A5 (fr)
DE (1)	DE3340214D2 (fr)
GB (1)	GB2129805B (fr)
HU (1)	HU187452B (fr)
NL (1)	NL8320114A (fr)
RO (1)	RO88377A (fr)
SE (1)	SE461433B (fr)
SU (1)	SU1318155A3 (fr)
WO (1)	WO1983003603A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN101618369B (zh) *	2009-07-24	2013-01-23	东北大学	一种赤铁矿低温浮选药剂及其制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2457674A (en) *	1944-12-02	1948-12-28	Rohm & Haas	Fungicidal compositions
US2695901A (en) *	1953-06-23	1954-11-30	Monsanto Chemicals	Thiocarbamyl cyanuryl derivatives
US2974156A (en) *	1958-08-29	1961-03-07	Rohm & Haas	Method for stabilization of manganese salts of alkylene bisdithiocarbamic acids and the products thereof
BE617407A (fr) *	1961-05-09
GB1038727A (en) *	1964-02-13	1966-08-10	Monsanto Chemicals	Vulcanisation process and novel bis(dithiocarbamates) for use therein
US3352815A (en) *	1965-03-08	1967-11-14	Ciba Geigy Corp	Aralkyl-phenyl nu-aryl-thiocarbamates
CH508339A (de) *	1969-05-08	1971-06-15	Ciba Geigy Ag	Mittel zur Bekämpfung von Insekten und Vertretern der Ordnung Acarina
BE788711A (fr) *	1971-09-13	1973-03-12	Azote & Prod Chim	Derives thiocarbamiques et compositions pesticides contenant ces derives

1982
- 1982-04-20 HU HU821205A patent/HU187452B/hu not_active IP Right Cessation
1983
- 1983-04-20 WO PCT/HU1983/000017 patent/WO1983003603A1/fr not_active Ceased
- 1983-04-20 AT AT0902183A patent/AT386927B/de not_active IP Right Cessation
- 1983-04-20 CH CH6923/83A patent/CH660482A5/de not_active IP Right Cessation
- 1983-04-20 NL NL8320114A patent/NL8320114A/nl unknown
- 1983-04-20 JP JP58501365A patent/JPS59500766A/ja active Pending
- 1983-04-20 US US06/568,210 patent/US4613615A/en not_active Expired - Fee Related
- 1983-04-20 DE DE83HU8300017T patent/DE3340214D2/de not_active Expired
- 1983-04-20 GB GB08333833A patent/GB2129805B/en not_active Expired
- 1983-12-16 RO RO83112908A patent/RO88377A/fr unknown
- 1983-12-19 SE SE8307028A patent/SE461433B/sv not_active IP Right Cessation
- 1983-12-19 SU SU833682651A patent/SU1318155A3/ru active

Also Published As

Publication number	Publication date
ATA902183A (de)	1988-04-15
JPS59500766A (ja)	1984-05-04
DE3340214D2 (en)	1984-05-17
SE8307028L (sv)	1983-12-19
RO88377A (fr)	1986-02-28
US4613615A (en)	1986-09-23
WO1983003603A1 (fr)	1983-10-27
GB8333833D0 (en)	1984-02-01
SE461433B (sv)	1990-02-19
AT386927B (de)	1988-11-10
SE8307028D0 (sv)	1983-12-19
GB2129805B (en)	1987-02-25
CH660482A5 (de)	1987-04-30
SU1318155A3 (ru)	1987-06-15
GB2129805A (en)	1984-05-23
HU187452B (en)	1986-01-28

Publication	Publication Date	Title
DE2808317C2 (fr)	1991-05-08
DE69637161T2 (de)	2007-10-25	Schädlingsbekämpfungsmittel für Landwirtschaft und Gartenbau und Verfahren zur Bekämpfung von Schädlingen
DE4033412A1 (de)	1992-04-23	Fungizide mittel auf basis von heterocyclisch substituierten sulfonen
DE3779836T2 (de)	1993-01-28	Iodopropargylcarbamat-derivate, herstellungsverfahren und fungizide mittel, die diese verbindungen enthalten.
CS221944B2 (en)	1983-04-29	Fungicide and/or bacteriocide means and method of making the active substances
NL8320114A (nl)	1984-03-01	Plantenbeschermingsmiddel.
DD149890A5 (de)	1981-08-05	Schimmelbekaempfungsmittel und-verfahren
CH637386A5 (de)	1983-07-29	Benzoxazol- und benzothiazolderivate.
US4195096A (en)	1980-03-25	Carboxylic amides as fungicides to eumycotina in phanerogamia plant life
PL117085B1 (en)	1981-07-31	Fungicide
US4325973A (en)	1982-04-20	Hydroxyalkyl amides as fungicides to eumycotina in phanerogamia plant life
US3242208A (en)	1966-03-22	Bis (trifluoromethyl) thio carbanilides
DD271256A1 (de)	1989-08-30	Fungizide mittel
DE1239311B (de)	1967-04-27	Verfahren zur Herstellung von biozid wirksamen Organozinnderivaten des s-Triazins
PL95242B1 (fr)	1977-09-30
EP0089651A1 (fr)	1983-09-28	Procédé de protection des plantes cultivées contre l'action des herbicides non-sélectifs
US4879314A (en)	1989-11-07	Dihaloformaldoxime
DE2112643C3 (de)	1981-02-19	Formamidin-Derivate und sie enthaltende Mittel
JPS60161907A (ja)	1985-08-23	腹足綱軟体動物及び蛞蝓状虫類の防除剤
DE69012921T2 (de)	1995-02-02	Azolidin-Derivate, Verfahren zu deren Herstellung und Fungizide für die Landwirtschaft und den Gartenbau.
JPS61286364A (ja)	1986-12-16	カルバミン酸ベンザルドキシム誘導体類
US4288455A (en)	1981-09-08	Method of controlling mollusc pest
US6013661A (en)	2000-01-11	Protection of crops against birds using a compound of phenylpyrazole type
US3780036A (en)	1973-12-18	Alkylthiocarbonates of s-dialkylamino halotriazines
SU651646A3 (ru)	1979-03-05	Гербицидный состав