UA80291C2 - Crystal modification of ii 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-3h-1,2,4-triazol-3-thion, process for the preparation thereof and microbicidal agent - Google Patents
Crystal modification of ii 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-3h-1,2,4-triazol-3-thion, process for the preparation thereof and microbicidal agent Download PDFInfo
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- UA80291C2 UA80291C2 UAA200501648A UA2005001648A UA80291C2 UA 80291 C2 UA80291 C2 UA 80291C2 UA A200501648 A UAA200501648 A UA A200501648A UA 2005001648 A UA2005001648 A UA 2005001648A UA 80291 C2 UA80291 C2 UA 80291C2
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- modification
- formula
- crystal
- chlorophenyl
- dihydro
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- 239000000454 talc Substances 0.000 description 1
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- 239000005936 tau-Fluvalinate Substances 0.000 description 1
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- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
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- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229940074152 thuringiensin Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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)
- Plural Heterocyclic Compounds (AREA)
- Developing Agents For Electrophotography (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10233171A DE10233171A1 (de) | 2002-07-22 | 2002-07-22 | Kristallmodifikation II des 2-[2-(Chlor-cyclopropyl)-3-(2-chlorphenyl)-2-hydroxy-propyl]-2,4dihydro-3H-1,2,4-triazol-3-thions |
PCT/EP2003/007473 WO2004008860A1 (de) | 2002-07-22 | 2003-07-10 | Kristallmodifikation ii des 2-[2-(1-chlor-cyclopropyl)-3-(2-chlorphenyl)-2-hydroxy-propyl]-2,4-dihydro-3h-1,2,4-triazol-3-thions |
Publications (1)
Publication Number | Publication Date |
---|---|
UA80291C2 true UA80291C2 (en) | 2007-09-10 |
Family
ID=30128215
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UAA200501648A UA80291C2 (en) | 2002-07-22 | 2003-10-07 | Crystal modification of ii 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-3h-1,2,4-triazol-3-thion, process for the preparation thereof and microbicidal agent |
Country Status (17)
Country | Link |
---|---|
US (1) | US7176226B2 (ko) |
EP (1) | EP1524905B1 (ko) |
JP (1) | JP4757490B2 (ko) |
KR (1) | KR20050025623A (ko) |
CN (1) | CN1681390B (ko) |
AR (1) | AR040505A1 (ko) |
AU (1) | AU2003246673B2 (ko) |
BR (1) | BR0312839A (ko) |
CA (1) | CA2492973C (ko) |
DE (1) | DE10233171A1 (ko) |
EA (1) | EA007384B1 (ko) |
IL (2) | IL166303A0 (ko) |
MX (1) | MX252778B (ko) |
PL (1) | PL206586B1 (ko) |
UA (1) | UA80291C2 (ko) |
WO (1) | WO2004008860A1 (ko) |
ZA (1) | ZA200500515B (ko) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR054777A1 (es) * | 2005-06-20 | 2007-07-18 | Basf Ag | Modificaciones cristalinas de piraclostrobina |
EP2703389A1 (en) * | 2008-06-17 | 2014-03-05 | Makhteshim Chemical Works Limited | Crystalline modifications of prothioconazole |
WO2019171161A1 (en) * | 2018-03-06 | 2019-09-12 | Upl Ltd | Improved process for preparation of intermediates |
CN110272393B (zh) * | 2018-03-13 | 2022-08-09 | 华东理工大学 | 丙硫菌唑溶剂化物及其制法和应用 |
CN110372617B (zh) * | 2019-08-08 | 2021-03-12 | 北京颖泰嘉和生物科技股份有限公司 | 一种药用组合物、丙硫菌唑的晶型及其制备方法、应用 |
CN110981822A (zh) * | 2019-11-27 | 2020-04-10 | 海利尔药业集团股份有限公司 | 一种丙硫菌唑ⅰ型晶型的制备方法 |
CN113019269B (zh) * | 2021-03-09 | 2022-11-04 | 江阴苏利化学股份有限公司 | 一种百菌清晶格转型装置及制备方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19528046A1 (de) | 1994-11-21 | 1996-05-23 | Bayer Ag | Triazolyl-Derivate |
DE19617282A1 (de) * | 1996-04-30 | 1997-11-06 | Bayer Ag | Triazolyl-mercaptide |
DE19619544A1 (de) * | 1996-05-15 | 1997-11-20 | Bayer Ag | Triazolyl-Disulfide |
DE19620407A1 (de) * | 1996-05-21 | 1997-11-27 | Bayer Ag | Thiocyano-triazolyl-Derivate |
DE19620590A1 (de) * | 1996-05-22 | 1997-11-27 | Bayer Ag | Sulfonyl-mercapto-triazolyl-Derivate |
DE19716257A1 (de) * | 1997-04-18 | 1998-10-22 | Bayer Ag | Fungizide Wirkstoffkombination |
ATE321031T1 (de) * | 1997-10-08 | 2006-04-15 | Bayer Cropscience Ag | Verfahren zur herstellung von triazolinthion- derivaten |
DE19744401A1 (de) * | 1997-10-08 | 1999-04-15 | Bayer Ag | Verfahren zur Herstellung von Triazolinthion-Derivaten |
DE19744400A1 (de) * | 1997-10-08 | 1999-04-15 | Bayer Ag | Verfahren zur Herstellung von Triazolinthion-Derivaten |
DE19744706A1 (de) * | 1997-10-10 | 1999-04-15 | Bayer Ag | Verfahren zur Herstellung von Triazolinthion-Derivaten |
DE19917617A1 (de) * | 1999-04-19 | 2000-10-26 | Bayer Ag | -(-)Enantiomeres des 2-[2-(1-Chlor-cyclopropyl)-3-(2-chlorphenyl) 2-hydroxy-propyl]-2,4-dihydro-[1,2,4]-triazol-3-thions |
DE19961603A1 (de) * | 1999-12-21 | 2001-06-28 | Bayer Ag | Verfahren zur Herstellung eines Triazolinthion-Derivates |
-
2002
- 2002-07-22 DE DE10233171A patent/DE10233171A1/de not_active Withdrawn
-
2003
- 2003-07-10 KR KR1020057000984A patent/KR20050025623A/ko not_active Application Discontinuation
- 2003-07-10 AU AU2003246673A patent/AU2003246673B2/en not_active Expired
- 2003-07-10 PL PL374797A patent/PL206586B1/pl unknown
- 2003-07-10 EA EA200500195A patent/EA007384B1/ru unknown
- 2003-07-10 EP EP03764967A patent/EP1524905B1/de not_active Revoked
- 2003-07-10 WO PCT/EP2003/007473 patent/WO2004008860A1/de active Application Filing
- 2003-07-10 US US10/521,715 patent/US7176226B2/en not_active Expired - Lifetime
- 2003-07-10 CN CN038224496A patent/CN1681390B/zh not_active Expired - Lifetime
- 2003-07-10 BR BR0312839-3A patent/BR0312839A/pt not_active Application Discontinuation
- 2003-07-10 JP JP2004522435A patent/JP4757490B2/ja not_active Expired - Fee Related
- 2003-07-10 MX MXPA05000853 patent/MX252778B/es active IP Right Grant
- 2003-07-10 IL IL16630303A patent/IL166303A0/xx unknown
- 2003-07-10 CA CA2492973A patent/CA2492973C/en not_active Expired - Lifetime
- 2003-07-18 AR AR20030102594A patent/AR040505A1/es not_active Application Discontinuation
- 2003-10-07 UA UAA200501648A patent/UA80291C2/uk unknown
-
2005
- 2005-01-13 IL IL166303A patent/IL166303A/en active IP Right Grant
- 2005-01-19 ZA ZA200500515A patent/ZA200500515B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
IL166303A (en) | 2010-06-30 |
CN1681390B (zh) | 2010-05-26 |
CA2492973C (en) | 2010-06-01 |
ZA200500515B (en) | 2006-03-29 |
MXPA05000853A (es) | 2005-04-19 |
AU2003246673B2 (en) | 2009-07-16 |
WO2004008860A1 (de) | 2004-01-29 |
AR040505A1 (es) | 2005-04-06 |
EA007384B1 (ru) | 2006-10-27 |
EA200500195A1 (ru) | 2005-06-30 |
KR20050025623A (ko) | 2005-03-14 |
AU2003246673A1 (en) | 2004-02-09 |
IL166303A0 (en) | 2006-01-15 |
BR0312839A (pt) | 2005-04-26 |
PL374797A1 (en) | 2005-10-31 |
JP4757490B2 (ja) | 2011-08-24 |
JP2006502994A (ja) | 2006-01-26 |
US7176226B2 (en) | 2007-02-13 |
PL206586B1 (pl) | 2010-08-31 |
EP1524905A1 (de) | 2005-04-27 |
CA2492973A1 (en) | 2004-01-29 |
EP1524905B1 (de) | 2010-05-26 |
DE10233171A1 (de) | 2004-02-12 |
CN1681390A (zh) | 2005-10-12 |
MX252778B (es) | 2007-12-18 |
US20060106080A1 (en) | 2006-05-18 |
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