SK282969B6 - Kryštálová modifikácia (4-cyklopropyl-6-metylpyrimidin-2-yl) fenylamínu, spôsob jej výroby, fungicídne prostriedky obsahujúce túto modifikáciu ako účinnú látku a ich použitie - Google Patents

Kryštálová modifikácia (4-cyklopropyl-6-metylpyrimidin-2-yl) fenylamínu, spôsob jej výroby, fungicídne prostriedky obsahujúce túto modifikáciu ako účinnú látku a ich použitie Download PDF

Info

Publication number: SK282969B6
Authority: SK; Slovakia
Prior art keywords: weak; cyclopropyl; phenylamine; methylpyrimidin; crystal modification
Prior art date: 1993-11-09

Application number

SK1330-94A

Other languages

English (en)

Slovak (sk)

Other versions

SK133094A3 (en

Inventor

Willy Baettig

Reinhard Georg Hanreich

Original Assignee

Novartis 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.)

1993-11-09

Filing date

1994-11-07

Publication date

2003-01-09

1994-11-07 Application filed by Novartis Ag filed Critical Novartis Ag

1995-06-07 Publication of SK133094A3 publication Critical patent/SK133094A3/sk

2003-01-09 Publication of SK282969B6 publication Critical patent/SK282969B6/sk

Links

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239000002518 antifoaming agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
BCOZLGOHQFNXBI-UHFFFAOYSA-M benzyl-bis(2-chloroethyl)-ethylazanium;bromide Chemical compound [Br-].ClCC[N+](CC)(CCCl)CC1=CC=CC=C1 BCOZLGOHQFNXBI-UHFFFAOYSA-M 0.000 description 1
235000021028 berry Nutrition 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
239000011449 brick Substances 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
229960000846 camphor Drugs 0.000 description 1
229930008380 camphor Natural products 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
XDSYAIICRRZSJX-UHFFFAOYSA-N carbamimidoyl(phenyl)azanium;hydrogen carbonate Chemical compound OC(O)=O.NC(N)=NC1=CC=CC=C1 XDSYAIICRRZSJX-UHFFFAOYSA-N 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
238000001311 chemical methods and process Methods 0.000 description 1
235000019693 cherries Nutrition 0.000 description 1
235000017803 cinnamon Nutrition 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
235000016213 coffee Nutrition 0.000 description 1
235000013353 coffee beverage Nutrition 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
229940124447 delivery agent Drugs 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
239000003599 detergent Substances 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
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000005452 ethyl sulfates Chemical class 0.000 description 1
238000000605 extraction Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000835 fiber Substances 0.000 description 1
238000011049 filling Methods 0.000 description 1
NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000011487 hemp Substances 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
235000008216 herbs Nutrition 0.000 description 1
239000012943 hotmelt Substances 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000002955 isolation Methods 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
238000005259 measurement Methods 0.000 description 1
125000002496 methyl group Chemical class [H]C([H])([H])* 0.000 description 1
150000005451 methyl sulfates Chemical class 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000003750 molluscacide Substances 0.000 description 1
230000002013 molluscicidal effect Effects 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
150000002888 oleic acid derivatives Chemical class 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
235000021017 pears Nutrition 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000006187 pill Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
235000021018 plums Nutrition 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
238000012545 processing Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000010992 reflux Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000019337 sorbitan trioleate Nutrition 0.000 description 1
229960000391 sorbitan trioleate Drugs 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
235000013599 spices Nutrition 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008117 stearic acid Chemical class 0.000 description 1
238000003756 stirring Methods 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
239000003760 tallow Substances 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- 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
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines

Landscapes

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

SK1330-94A 1993-11-09 1994-11-07 Kryštálová modifikácia (4-cyklopropyl-6-metylpyrimidin-2-yl) fenylamínu, spôsob jej výroby, fungicídne prostriedky obsahujúce túto modifikáciu ako účinnú látku a ich použitie SK282969B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH336893		1993-11-09
CH239394		1994-07-28

Publications (2)

Publication Number	Publication Date
SK133094A3 SK133094A3 (en)	1995-06-07
SK282969B6 true SK282969B6 (sk)	2003-01-09

Family

ID=25690336

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1330-94A SK282969B6 (sk)	1993-11-09	1994-11-07	Kryštálová modifikácia (4-cyklopropyl-6-metylpyrimidin-2-yl) fenylamínu, spôsob jej výroby, fungicídne prostriedky obsahujúce túto modifikáciu ako účinnú látku a ich použitie

Country Status (22)

Country	Link
US (1)	US5830899A (fr)
EP (1)	EP0655441B1 (fr)
JP (1)	JP3617015B2 (fr)
KR (1)	KR100349994B1 (fr)
CN (1)	CN1053897C (fr)
AT (1)	ATE212337T1 (fr)
AU (1)	AU689805B2 (fr)
BR (1)	BR9404388A (fr)
CA (1)	CA2135251C (fr)
CZ (1)	CZ291977B6 (fr)
DE (1)	DE59410036D1 (fr)
DK (1)	DK0655441T3 (fr)
ES (1)	ES2171443T3 (fr)
FI (1)	FI112215B (fr)
HU (1)	HU213946B (fr)
IL (1)	IL111537A (fr)
NO (1)	NO306551B1 (fr)
PL (1)	PL179802B1 (fr)
PT (1)	PT655441E (fr)
RU (1)	RU2145601C1 (fr)
SK (1)	SK282969B6 (fr)
UA (1)	UA39175C2 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CO4940418A1 (es) *	1997-07-18	2000-07-24	Novartis Ag	Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso
GB0706044D0 (en) *	2007-03-28	2007-05-09	Syngenta Ltd	C0-Crystals
CN101311170B (zh)	2007-05-25	2010-09-15	中国中化股份有限公司	取代嘧啶醚类化合物及其应用
GB0817976D0 (en) *	2008-10-01	2008-11-05	Syngenta Ltd	Co-crystals
CN101906075B (zh)	2009-06-05	2012-11-07	中国中化股份有限公司	含取代苯胺基嘧啶基团的e-型苯基丙烯酸酯类化合物及其应用
GB201006326D0 (en)	2010-04-15	2010-06-02	Syngenta Ltd	Formulation
FR2965563B1 (fr)	2010-09-30	2015-05-15	Roquette Freres	Pastilles de dianhydrohexitols de grande fluidite et non mottantes
KR102116254B1 (ko)	2019-01-28	2020-05-28	서진영	프리사이즈 절단가능한 스폰지 재단장치

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4810789A (en) *	1987-08-28	1989-03-07	Bristol-Myers Company	Process for buspirone hydrochloride polymorphic crystalline form conversion
US5153200A (en) *	1987-09-28	1992-10-06	Ciba-Geigy Corporation	Pesticides
ES2054867T3 (es) *	1987-09-28	1994-08-16	Ciba Geigy Ag	Plaguicidas y pesticidas.

1994
- 1994-11-01 ES ES94810626T patent/ES2171443T3/es not_active Expired - Lifetime
- 1994-11-01 DE DE59410036T patent/DE59410036D1/de not_active Expired - Lifetime
- 1994-11-01 EP EP94810626A patent/EP0655441B1/fr not_active Expired - Lifetime
- 1994-11-01 AT AT94810626T patent/ATE212337T1/de active
- 1994-11-01 PT PT94810626T patent/PT655441E/pt unknown
- 1994-11-01 DK DK94810626T patent/DK0655441T3/da active
- 1994-11-04 UA UA94115997A patent/UA39175C2/uk unknown
- 1994-11-07 CA CA002135251A patent/CA2135251C/fr not_active Expired - Lifetime
- 1994-11-07 CZ CZ19942730A patent/CZ291977B6/cs not_active IP Right Cessation
- 1994-11-07 IL IL11153794A patent/IL111537A/en not_active IP Right Cessation
- 1994-11-07 FI FI945231A patent/FI112215B/fi not_active IP Right Cessation
- 1994-11-07 PL PL94305740A patent/PL179802B1/pl unknown
- 1994-11-07 SK SK1330-94A patent/SK282969B6/sk not_active IP Right Cessation
- 1994-11-08 AU AU77688/94A patent/AU689805B2/en not_active Expired
- 1994-11-08 BR BR9404388A patent/BR9404388A/pt not_active IP Right Cessation
- 1994-11-08 NO NO944253A patent/NO306551B1/no not_active IP Right Cessation
- 1994-11-08 KR KR1019940029519A patent/KR100349994B1/ko not_active Expired - Lifetime
- 1994-11-08 HU HU9403214A patent/HU213946B/hu unknown
- 1994-11-09 CN CN94118186A patent/CN1053897C/zh not_active Expired - Lifetime
- 1994-11-09 JP JP30040194A patent/JP3617015B2/ja not_active Expired - Lifetime
- 1994-11-09 RU RU94040724A patent/RU2145601C1/ru active
1997
- 1997-08-12 US US08/909,491 patent/US5830899A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
JP3617015B2 (ja)	2005-02-02
KR950014078A (ko)	1995-06-15
IL111537A0 (en)	1995-01-24
US5830899A (en)	1998-11-03
JPH07188183A (ja)	1995-07-25
RU94040724A (ru)	1996-10-10
DK0655441T3 (da)	2002-05-06
CN1105995A (zh)	1995-08-02
FI112215B (fi)	2003-11-14
CZ291977B6 (cs)	2003-06-18
CA2135251C (fr)	2005-12-20
HK1008961A1 (en)	1999-05-21
BR9404388A (pt)	1995-07-04
NO944253L (no)	1995-05-10
EP0655441A1 (fr)	1995-05-31
FI945231L (fi)	1995-05-10
AU689805B2 (en)	1998-04-09
FI945231A0 (fi)	1994-11-07
HU9403214D0 (en)	1995-01-30
UA39175C2 (uk)	2001-06-15
RU2145601C1 (ru)	2000-02-20
PL305740A1 (en)	1995-05-15
HUT68779A (en)	1995-07-28
SK133094A3 (en)	1995-06-07
KR100349994B1 (ko)	2002-12-16
PL179802B1 (pl)	2000-10-31
CA2135251A1 (fr)	1995-05-10
NO306551B1 (no)	1999-11-22
AU7768894A (en)	1995-05-18
HU213946B (en)	1997-11-28
ES2171443T3 (es)	2002-09-16
NO944253D0 (no)	1994-11-08
CZ273094A3 (en)	1995-05-17
EP0655441B1 (fr)	2002-01-23
ATE212337T1 (de)	2002-02-15
IL111537A (en)	2001-06-14
DE59410036D1 (de)	2002-03-14
CN1053897C (zh)	2000-06-28
PT655441E (pt)	2002-06-28

Legal Events

Date	Code	Title	Description
2015-01-07	MK4A	Expiry of patent	Expiry date: 20141107

Publication	Publication Date	Title
EP0206999B1 (fr)	1991-08-14	Substance microbicide
KR970001478B1 (ko)	1997-02-06	살균제
EP0139613A1 (fr)	1985-05-02	Dérivés de la N-(nitro-2 phényl) amino-4 pyrimidine, leur préparation et leur application
CS244935B2 (en)	1986-08-14	Agent for plants diseases suppresion
EP0133247B1 (fr)	1989-12-13	Dérivés de N-aminométhyl-3-phényl-4-cyanopyrrole, leur préparation et leur utilisation comme microbicide
EP0310558A2 (fr)	1989-04-05	Agent microbicide
SK76794A3 (en)	1995-01-12	Microbicidal agent for protection of plants, its using method of suppression of plants illness and herbal propagation material
SK133094A3 (en)	1995-06-07	Crystal modification of (4-cyclopropyl-6-methyl-2-pyrimidinyl) phenylamine, method of its production fungicidal agents containing this modification as effective matter and their use
JPH01157964A (ja)	1989-06-21	殺菌性ピリジルシクロプロパンカルボキサミジン
US4687861A (en)	1987-08-18	Microbicidal compositions
EP0096142B1 (fr)	1989-01-18	Sulfényl pyrrole microbicide
RO112566B1 (ro)	1997-11-28	Metoda pentru combaterea insectelor si de protectie a materialului de inmultire a plantelor
EP0386681A1 (fr)	1990-09-12	Dérivés de 3-aryl-4-cyano-pyrrole, procédé pour leur préparation et agents microbiocide les contenant
BE1008752A3 (fr)	1996-07-02	Procede et agent de lutte antiparasitaire.
HU189598B (en)	1986-07-28	Fungicidal, bactericidal and plant growth regulating compositions comprising imidazolyl-propionitrile-derivatives as active substance and process for preparing imidazolyl-propionitrile derivatives
CH677664A5 (fr)	1991-06-14
RU2070197C1 (ru)	1996-12-10	Производные тиазолил-5-карбонамида, фунгицидное средство для борьбы с грибными болезнями растений, способ борьбы с грибными болезнями растений
JP3624209B2 (ja)	2005-03-02	農園芸用殺菌剤
NO127152B (fr)	1973-05-14
JPH04211668A (ja)	1992-08-03	殺微生物剤
HK1008961B (en)	2002-12-20	Crystalline modification of (4-cyclopropyl-6-methyl-pyrimidin-2-yl)-phenyl-amine, and process for its preparation
EP0215307A2 (fr)	1987-03-25	Dérivés de la pyrimidine, leur procédé de préparation et leur application en tant que microbicides
PL152669B1 (pl)	1991-01-31	Środek mikrobobójczy
JPS59161350A (ja)	1984-09-12	Ｎ−〔２−（１，２−ジクロロビニルオキシ）−フエニルスルホニル〕（チオ）尿素、その製造方法及び殺微生物剤