DD144499A5 - Schimmelbekaempfungsmittel - Google Patents

Schimmelbekaempfungsmittel Download PDF

Info

Publication number: DD144499A5
Authority: DD; German Democratic Republic
Prior art keywords: methyl; item; group; chlorine; mol
Prior art date: 1977-10-26

Application number

DD78208697A

Other languages

German (de)

English (en)

Inventor

Francis H Walker

Don R Baker

Original Assignee

Stauffer Chemical 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.)

1977-10-26

Filing date

1978-10-26

Publication date

1980-10-22

1977-10-26 Priority claimed from US05/845,513 external-priority patent/US4154849A/en

1977-10-26 Priority claimed from US05/845,514 external-priority patent/US4168319A/en

1978-10-26 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1980-10-22 Publication of DD144499A5 publication Critical patent/DD144499A5/de

Links

150000001875 compounds Chemical class 0.000 claims description 31
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 31
239000000203 mixture Substances 0.000 claims description 25
239000000460 chlorine Substances 0.000 claims description 17
239000003795 chemical substances by application Substances 0.000 claims description 16
229910052801 chlorine Inorganic materials 0.000 claims description 16
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 13
229910052794 bromium Inorganic materials 0.000 claims description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
-1 chloro, bromo, thiocyano Chemical group 0.000 claims description 3
125000005031 thiocyano group Chemical group S(C#N)* 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims 10
125000001246 bromo group Chemical group Br* 0.000 claims 2
125000004093 cyano group Chemical group *C#N 0.000 claims 1
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
239000002253 acid Substances 0.000 description 12
238000005481 NMR spectroscopy Methods 0.000 description 10
238000002844 melting Methods 0.000 description 10
230000008018 melting Effects 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 9
150000001263 acyl chlorides Chemical class 0.000 description 8
239000002904 solvent Substances 0.000 description 8
238000010183 spectrum analysis Methods 0.000 description 8
230000000361 pesticidal effect Effects 0.000 description 7
238000001816 cooling Methods 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
244000046052 Phaseolus vulgaris Species 0.000 description 5
235000010627 Phaseolus vulgaris Nutrition 0.000 description 5
239000000575 pesticide Substances 0.000 description 5
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 5
239000007787 solid Substances 0.000 description 5
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
241000233866 Fungi Species 0.000 description 4
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
150000001408 amides Chemical class 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 4
DVECBJCOGJRVPX-UHFFFAOYSA-N butyryl chloride Chemical compound CCCC(Cl)=O DVECBJCOGJRVPX-UHFFFAOYSA-N 0.000 description 4
235000011089 carbon dioxide Nutrition 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
238000003756 stirring Methods 0.000 description 4
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
241000221785 Erysiphales Species 0.000 description 3
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
238000006467 substitution reaction Methods 0.000 description 3
239000000725 suspension Substances 0.000 description 3
229950011008 tetrachloroethylene Drugs 0.000 description 3
FDQQNNZKEJIHMS-UHFFFAOYSA-N 3,4,5-trimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1C FDQQNNZKEJIHMS-UHFFFAOYSA-N 0.000 description 2
WMUWDPLTTLJNPE-UHFFFAOYSA-N 4-bromo-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1Br WMUWDPLTTLJNPE-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
229920001213 Polysorbate 20 Polymers 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
241000607479 Yersinia pestis Species 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
125000001931 aliphatic group Chemical class 0.000 description 2
229910052786 argon Inorganic materials 0.000 description 2
239000007810 chemical reaction solvent Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000007789 gas Substances 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
229910052943 magnesium sulfate Inorganic materials 0.000 description 2
235000019341 magnesium sulphate Nutrition 0.000 description 2
150000007530 organic bases Chemical class 0.000 description 2
239000012044 organic layer Substances 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
238000010926 purge Methods 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
OLUWJEIVKCVRNC-UHFFFAOYSA-N 2-(4-bromo-3,5-dimethylphenoxy)butanoic acid Chemical compound CCC(C(O)=O)OC1=CC(C)=C(Br)C(C)=C1 OLUWJEIVKCVRNC-UHFFFAOYSA-N 0.000 description 1
MHDPSHKDNCZMAW-UHFFFAOYSA-N 2-(4-bromo-3,5-dimethylphenoxy)butanoyl chloride Chemical compound CCC(C(Cl)=O)OC1=CC(C)=C(Br)C(C)=C1 MHDPSHKDNCZMAW-UHFFFAOYSA-N 0.000 description 1
YAQLSKVCTLCIIE-UHFFFAOYSA-M 2-bromobutanoate Chemical compound CCC(Br)C([O-])=O YAQLSKVCTLCIIE-UHFFFAOYSA-M 0.000 description 1
YAQLSKVCTLCIIE-UHFFFAOYSA-N 2-bromobutyric acid Chemical compound CCC(Br)C(O)=O YAQLSKVCTLCIIE-UHFFFAOYSA-N 0.000 description 1
OSDLLIBGSJNGJE-UHFFFAOYSA-N 4-chloro-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1Cl OSDLLIBGSJNGJE-UHFFFAOYSA-N 0.000 description 1
239000004604 Blowing Agent Substances 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
229910014033 C-OH Inorganic materials 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
229910014570 C—OH Inorganic materials 0.000 description 1
239000004338 Dichlorodifluoromethane Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
235000002096 Vicia faba var. equina Nutrition 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000001514 detection method Methods 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
244000013123 dwarf bean Species 0.000 description 1
235000005489 dwarf bean Nutrition 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
XWBDWHCCBGMXKG-UHFFFAOYSA-N ethanamine;hydron;chloride Chemical compound Cl.CCN XWBDWHCCBGMXKG-UHFFFAOYSA-N 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000295 fuel oil Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
CQOYFACEVXRLJG-UHFFFAOYSA-N pent-2-yn-1-amine Chemical compound CCC#CCN CQOYFACEVXRLJG-UHFFFAOYSA-N 0.000 description 1
239000012071 phase Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000008159 sesame oil Substances 0.000 description 1
235000011803 sesame oil Nutrition 0.000 description 1
239000012312 sodium hydride Chemical class 0.000 description 1
229910000104 sodium hydride Chemical class 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; 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
- A01N47/40—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/48—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —S—C≡N groups

Landscapes

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

DD78208697A 1977-10-26 1978-10-26 Schimmelbekaempfungsmittel DD144499A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US05/845,513 US4154849A (en)	1977-10-26	1977-10-26	N-Cyano-2-(substituted phenoxy) butyramides and their use as mildewicides
US05/845,514 US4168319A (en)	1977-10-26	1977-10-26	N-alkynyl-2-(substituted phenoxy) butyramides and their use as mildewicides

Publications (1)

Publication Number	Publication Date
DD144499A5 true DD144499A5 (de)	1980-10-22

Family

ID=27126583

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD78220079A DD149890A5 (de)	1977-10-26	1978-10-26	Schimmelbekaempfungsmittel und-verfahren
DD78208697A DD144499A5 (de)	1977-10-26	1978-10-26	Schimmelbekaempfungsmittel

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
DD78220079A DD149890A5 (de)	1977-10-26	1978-10-26	Schimmelbekaempfungsmittel und-verfahren

Country Status (17)

Country	Link
EP (1)	EP0001721B1 (ro)
JP (1)	JPS5473743A (ro)
AR (1)	AR220917A1 (ro)
AU (1)	AU522381B2 (ro)
BR (1)	BR7807046A (ro)
CA (1)	CA1117961A (ro)
DD (2)	DD149890A5 (ro)
DE (1)	DE2861093D1 (ro)
DK (1)	DK477978A (ro)
EG (1)	EG13498A (ro)
GR (1)	GR72949B (ro)
IL (1)	IL62884A0 (ro)
NZ (1)	NZ188730A (ro)
PH (1)	PH13317A (ro)
PT (1)	PT68701B (ro)
RO (3)	RO81038A (ro)
YU (1)	YU250378A (ro)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2446812A1 (fr) *	1979-01-16	1980-08-14	Produits Ind Cie Fse	Phenoxy- et thiophenoxynitriles et leurs applications en tant qu'herbicides
GB2108498B (en) *	1981-10-20	1985-11-06	Ube Industries	Phenoxyalkylamide derivative, process for preparing the same, herbicidal composition containing the same and method for controlling weeds by the use of the same
EP0262393B1 (de) *	1986-08-29	1993-01-07	Shell Internationale Researchmaatschappij B.V.	Aryloxycarbonsäurederivate, ihre Herstellung und Verwendung
US5942640A (en) *	1998-04-20	1999-08-24	American Cyanamid Company	Process for the manufacture of N-(1-cyanoalkyl)-2-phenoxypropionamide derivatives
GB0227555D0 (en)	2002-11-26	2002-12-31	Syngenta Ltd	Fungicides
GB0227556D0 (en)	2002-11-26	2002-12-31	Syngenta Ltd	Fungicides
GB0227551D0 (en) *	2002-11-26	2002-12-31	Syngenta Ltd	Fungicides
GB0227558D0 (en) *	2002-11-26	2002-12-31	Syngenta Ltd	Fungicides
GB0227557D0 (en) *	2002-11-26	2002-12-31	Syngenta Ltd	Fungicides
GB0227554D0 (en) *	2002-11-26	2002-12-31	Syngenta Ltd	Fungicides
GB0312863D0 (en)	2003-06-04	2003-07-09	Syngenta Ltd	Fungicides

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3557209A (en) *	1967-10-18	1971-01-19	Velsicol Chemical Corp	Phenoxyacetamides
US3932168A (en) *	1971-11-17	1976-01-13	Abbott Laboratories	Substituted aryloxyacetamido nitrile derivatives as carbohydrate deposition agents
US4052432A (en) *	1974-11-18	1977-10-04	Stauffer Chemical Company	N-(1,1 Substituted acetonitrilo)-α-(3,5-substituted phenoxy) alkyl amides
US4051184A (en) *	1975-04-26	1977-09-27	Stauffer Chemical Company	N-(1,1 substituted propynyl)-α(3,5-substituted phenoxy) alkyl amides and their use as herbicides
US4001427A (en) *	1975-06-26	1977-01-04	Stauffer Chemical Company	N-dimethylacetonitrile-α-(substituted phenoxy) alkylamides and their use as miticides
US3971850A (en) *	1975-06-30	1976-07-27	Stauffer Chemical Company	N-substituted-N-(1-substituted-1-methyl-2-propynyl)-α-(substituted phenoxy) alkylamides and their use as miticides

1978
- 1978-10-24 AR AR274207A patent/AR220917A1/es active
- 1978-10-25 PH PH21733A patent/PH13317A/en unknown
- 1978-10-25 BR BR7807046A patent/BR7807046A/pt unknown
- 1978-10-25 DE DE7878300544T patent/DE2861093D1/de not_active Expired
- 1978-10-25 NZ NZ188730A patent/NZ188730A/xx unknown
- 1978-10-25 GR GR57510A patent/GR72949B/el unknown
- 1978-10-25 AU AU41033/78A patent/AU522381B2/en not_active Expired
- 1978-10-25 PT PT68701A patent/PT68701B/pt unknown
- 1978-10-25 EG EG627/78A patent/EG13498A/xx active
- 1978-10-25 EP EP78300544A patent/EP0001721B1/en not_active Expired
- 1978-10-26 RO RO78102395A patent/RO81038A/ro unknown
- 1978-10-26 DK DK477978A patent/DK477978A/da not_active Application Discontinuation
- 1978-10-26 DD DD78220079A patent/DD149890A5/de unknown
- 1978-10-26 RO RO7895508A patent/RO75384A/ro unknown
- 1978-10-26 RO RO107591A patent/RO85275B/ro unknown
- 1978-10-26 CA CA000314405A patent/CA1117961A/en not_active Expired
- 1978-10-26 YU YU02503/78A patent/YU250378A/xx unknown
- 1978-10-26 JP JP13106778A patent/JPS5473743A/ja active Pending
- 1978-10-26 DD DD78208697A patent/DD144499A5/de unknown
1981
- 1981-05-15 IL IL62884A patent/IL62884A0/xx unknown

Also Published As

Publication number	Publication date
GR72949B (ro)	1984-01-17
DK477978A (da)	1979-04-27
EP0001721A2 (en)	1979-05-02
RO81038B (ro)	1983-01-30
CA1117961A (en)	1982-02-09
DD149890A5 (de)	1981-08-05
AU522381B2 (en)	1982-06-03
DE2861093D1 (en)	1981-12-03
RO85275B (ro)	1984-10-30
PT68701A (en)	1978-11-01
RO81038A (ro)	1983-02-01
BR7807046A (pt)	1979-05-08
PH13317A (en)	1980-03-13
EP0001721B1 (en)	1981-09-16
EG13498A (en)	1982-09-30
EP0001721A3 (en)	1979-05-16
JPS5473743A (en)	1979-06-13
NZ188730A (en)	1980-05-08
RO75384A (ro)	1980-11-30
AU4103378A (en)	1980-05-01
AR220917A1 (es)	1980-12-15
RO85275A (ro)	1984-09-29
IL62884A0 (en)	1981-07-31
YU250378A (en)	1983-04-30
PT68701B (pt)	1981-06-11

Publication	Publication Date	Title
DE69028461T2 (de)	1997-02-06	Triazin-derivate und unkrautvertilgungsmittel daraus
DE112020001084T5 (de)	2022-01-27	Arylsulfid mit Benzylaminstruktur und dessen Syntheseverfahren und Anwendung
DE2743767A1 (de)	1979-04-12	Diastereomere triazolyl-0,n-acetale, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
DD144499A5 (de)	1980-10-22	Schimmelbekaempfungsmittel
CH640108A5 (de)	1983-12-30	Unkrautvernichtungsmittel.
DE2543888C3 (de)	1978-12-14	l-Phenyl-S-alkyl-S-benzylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0037971B1 (de)	1983-12-21	Trisubstituierte Cyanguanidine, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
DE2619303A1 (de)	1976-11-18	Neue schwefelhaltige bisformamidine, verfahren zu ihrer herstellung und verwendung derselben sowie diese enthaltende land-, garten- und forstwirtschaftliche chemikalien
EP0072528B1 (de)	1986-05-14	(Thio-) Harnstoffe, ein Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenschutzmittel
EP0158074A1 (de)	1985-10-16	Mikrobizide Mittel
EP0029908B1 (de)	1982-12-22	6H-1,2,4,6-Thiatriazin-1,1-dioxide, Herbizide, die diese Verbindungen enthalten, ihre Anwendung als Herbizide und Verfahren zu ihrer Herstellung
CH644854A5 (de)	1984-08-31	Salze von thiazolyliden-oxo-propionitrilen, insektizides mittel, enthaltend diese salze sowie verfahren zu ihrer herstellung.
EP0040740A2 (de)	1981-12-02	Aminopropanol-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0094539B1 (de)	1985-08-21	Halogenpropargylformamide
DD248357A5 (de)	1987-08-05	Verfahren zur herstellung von 9,10-phenonthrendion-derivaten
DD157292A5 (de)	1982-11-03	Mittel zur behandlung von pilzinfektionen
DE2557406A1 (de)	1976-07-08	Neue thioharnstoffverbindungen, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE1543614B2 (de)	1975-03-20	N-(Trihalogenmethylthio)-N-trifluor-methylamino-benzamide, Verfahren zu deren Herstellung und deren Verwendung
DE2328728A1 (de)	1975-01-09	Systemisch-fungizide mittel
DE3639901A1 (de)	1988-06-01	Saccharin-salze von substituierten aminen
EP0003975B1 (de)	1981-05-13	Dichlormaleinsäurediamid-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0046557B1 (de)	1984-02-22	N-Sulfenylierte Harnstoffe, Verfahren zu ihrer Herstellung, diese enthaltende fungizide Mittel und ihre Verwendung
EP0023976A1 (de)	1981-02-18	N-Aryl-N'-acryloyl-ureide, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Mikrobizide
DE2163381A1 (de)	1972-07-27	Herbizide Komposition
DE2453210A1 (de)	1976-05-13	Fungizides mittel