CN1226237A - 氰硫基-三唑基衍生物及其作为杀微生物剂的用途 - Google Patents
氰硫基-三唑基衍生物及其作为杀微生物剂的用途 Download PDFInfo
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- CN1226237A CN1226237A CN97196629A CN97196629A CN1226237A CN 1226237 A CN1226237 A CN 1226237A CN 97196629 A CN97196629 A CN 97196629A CN 97196629 A CN97196629 A CN 97196629A CN 1226237 A CN1226237 A CN 1226237A
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- carbon atom
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- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- JYQUHIFYBATCCY-UHFFFAOYSA-N quinalphos Chemical compound C1=CC=CC2=NC(OP(=S)(OCC)OCC)=CN=C21 JYQUHIFYBATCCY-UHFFFAOYSA-N 0.000 description 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 description 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical class CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 201000010153 skin papilloma Diseases 0.000 description 1
- 210000004894 snout Anatomy 0.000 description 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229960005137 succinic acid Drugs 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
- 238000003419 tautomerization reaction Methods 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
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-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
- 239000004753 textile Substances 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-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
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-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
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-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
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-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
- 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
- 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
- 210000002700 urine Anatomy 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin 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-IMTORBKUSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 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
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon 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
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
R6 | R7 | X1 m |
-CH3 | -CH3 | 2-Cl |
-CH3 | -CH3 | 2,3-Cl2 |
-CH3 | -CH3 | 4-CF3 |
-CH3 | -CH3 | 4-OCF3 |
-CH3 | -CH3 | 4-Cl |
R8 | R9 | X2 p | n |
-CH3 | -CH3 | 4-Br | 0 |
-CH3 | -CH3 | 4-F | 0 |
-CH3 | -CH3 | 2,4-Cl3 | 0 |
-CH3 | H | 4-Cl | 0 |
-CH3 | -CH3 | - | 0 |
-CH3 | -CH3 | 4-CH3 | 0 |
-CH3 | -CH3 | 2-F,4-Cl | 0 |
-C2H5 | H | 4-Cl | 0 |
-C2H5 | -C2H5 | 4-Cl | 0 |
-C3H2-n | H | 4-Cl | 0 |
-C2H5 | H | 2,4-Cl2 | 0 |
-C2H5 | H | 4-F | 0 |
-C2H5 | H | 4-Br | 0 |
-C2H5 | H | 4-NO2 | 0 |
-C2H5 | H | 4-C4H9-t | 0 |
-C3H7-i | H | 4-Cl | 0 |
-C5H11-n | H | 4-Cl | 0 |
-CH3 | -CH3 | 4-CN | 0 |
-CH3 | -CH3 | 4-C4H9-t | 0 |
-C4H9-n | H | 4-Cl | 0 |
-C4H9-i | H | 4-Cl | 0 |
-CH3 | -C2H5 | 4-Cl | 0 |
R8 | R9 | X2 p | n |
-CH3 | -CH3 | 4-OCH3 | 0 |
-CH3 | -CH3 | 2-OCH3 | 0 |
-CH3 | -CH3 | 2-CF3 | 0 |
-CH3 | -CH3 | 4-CF3 | 0 |
-CH3 | -CH3 | 2-OCF3 | 0 |
-CH3 | -CH3 | 2-OCHF2 | 0 |
-CH3 | -CH3 | 4-OCF3 | 0 |
-CH3 | -CH3 | 4-Br | 1 |
-CH3 | -CH3 | 4-F | 1 |
-CH3 | -CH3 | 2,4-Cl2 | 1 |
-CH3 | H | 4-Cl | 1 |
-CH3 | -CH3 | - | 1 |
-CH3 | -CH3 | 4-CH3 | 1 |
-CH3 | -CH3 | 2-F,4-Cl | 1 |
-C2H5 | H | 4-Cl | 1 |
-C2H5 | -C2H5 | 4-Cl | 1 |
-C3H7-n | H | 4-Cl | 1 |
-C2H5 | H | 2,4-Cl2 | 1 |
-C2H3 | H | 4-F | 1 |
-C2H5 | H | 4-Br | 1 |
-C2H5 | H | 4-NO2 | 1 |
-C2H5 | H | 4-C4H9-t | 1 |
-C3H7-i | H | 4-Cl | 1 |
-C5H11-n | H | 4-Cl | 1 |
-CH3 | -CH3 | 4-CN | 1 |
R8 | R9 | X2 p | n |
-CH3 | -CH3 | 4-C4H9-t | 1 |
-C4H9-n | H | 4-Cl | 1 |
-CH3 | -CH3 | 4-Cl | 1 |
-CH3 | -CH3 | 4-OCH3 | 1 |
-CH3 | -CH3 | 2-OCH3 | 1 |
-CH3 | -CH3 | 2-CF3 | 1 |
-CH3 | -CH3 | 4-CF3 | 1 |
-CH3 | -CH3 | 2-OCF3 | 1 |
-CH3 | -CH3 | 2-OCHF2 | 1 |
-CH3 | -CH3 | 4-OCF3 | 1 |
-CH3 | -CH3 | 2-Cl | 0 |
-CH3 | -CH3 | 2,3-Cl2 | 0 |
-CH3 | -CH3 | 2-Cl | 1 |
-CH3 | -CH3 | 4-Cl | 0 |
X3 q | Y1 | R11 |
4-Cl | CH2 | H |
4-CF3 | CH2 | H |
4-OCF3 | CH2 | H |
2,4-Cl2 | CH2 | H |
4-CH3 | CH2 | H |
2-Cl | CH2 | H |
2-F | CH2 | H |
4-F | CH2 | H |
2-OCHF2 | CH2 | H |
4-Cl | O | H |
4-CF3 | O | H |
4-OCF3 | O | H |
2,4-Cl2 | O | H |
4-CH3 | O | H |
2-Cl | O | H |
2-F | O | H |
4-F | O | H |
2-OCHF2 | O | H |
X3 q | Y1 | R11 |
4-Cl | - | H |
4-CF3 | - | H |
4-OCF3 | - | H |
2,4-Cl2 | - | H |
4-CH3 | - | H |
2-Cl | - | H |
2-F | - | H |
4-F | - | H |
2-OCHF2 | - | H |
4-Cl | CH2 | -CH3 |
4-CF3 | CH2 | -CH3 |
4-OCF3 | CH2 | -CH3 |
2,4-Cl2 | CH2 | -CH3 |
4-CH3 | CH2 | -CH3 |
2-Cl | CH2 | -CH3 |
2-F | CH2 | -CH3 |
4-F | CH2 | -CH3 |
2-OCHF2 | CH2 | -CH3 |
4-Cl | O | -CH3 |
4-CF3 | O | -CH3 |
2,4-Cl2 | O | -CH3 |
4-OCF3 | O | -CH3 |
2-F | O | -CH3 |
X6 t | R13 |
2,4-Cl2 | -CH2-O-CF2-CH3 |
4-Cl | -CH3-O-CF2-CHF2 |
2,4-Cl2 | -CH2-O-CF3 |
4-F | -CH2-O-CF2-CHF2 |
2-Cl | -CH2-O-CF2-CHF2 |
2,4-Cl2 | -CH2-CF3 |
2,4-Cl2 | -CF2-CF3 |
2,4-Cl2 | -C3H7-n |
Claims (6)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19620407.0 | 1996-05-21 | ||
DE19620407A DE19620407A1 (de) | 1996-05-21 | 1996-05-21 | Thiocyano-triazolyl-Derivate |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1226237A true CN1226237A (zh) | 1999-08-18 |
CN1158267C CN1158267C (zh) | 2004-07-21 |
Family
ID=7794885
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB97196629XA Expired - Lifetime CN1158267C (zh) | 1996-05-21 | 1997-05-09 | 氰硫基-三唑基衍生物及其作为杀微生物剂的用途 |
Country Status (9)
Country | Link |
---|---|
US (1) | US6166059A (zh) |
EP (1) | EP0901478B1 (zh) |
JP (1) | JP4218984B2 (zh) |
CN (1) | CN1158267C (zh) |
AU (1) | AU2952997A (zh) |
BR (1) | BR9709107A (zh) |
DE (2) | DE19620407A1 (zh) |
ES (1) | ES2205222T3 (zh) |
WO (1) | WO1997044331A1 (zh) |
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CN102458124A (zh) * | 2009-06-16 | 2012-05-16 | 巴斯夫欧洲公司 | 杀真菌混合物 |
CN102802416A (zh) * | 2009-06-18 | 2012-11-28 | 巴斯夫欧洲公司 | 杀真菌混合物 |
CN103596934A (zh) * | 2011-05-31 | 2014-02-19 | 株式会社吴羽 | 三氮杂茂化合物、及其运用 |
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WO2005090320A2 (en) * | 2004-03-12 | 2005-09-29 | Wyeth | Triazole derivatives and method of using the same to treat hiv infections |
EP2224812A2 (de) * | 2007-12-19 | 2010-09-08 | Basf Se | Azolylmethyloxirane, ihre verwendung sowie sie enthaltende mittel |
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US20100273651A1 (en) * | 2007-12-19 | 2010-10-28 | Basf Se | Azolylmethyloxiranes, use Thereof and Agents Containing the Same |
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AR076427A1 (es) * | 2009-04-24 | 2011-06-08 | Basf Se | Compuestos de triazol que llevan un sustituyente de azufre ii |
WO2010142779A1 (en) | 2009-06-12 | 2010-12-16 | Basf Se | Antifungal 1,2,4-triazolyl derivatives having a 5- sulfur substituent |
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- 1996-05-21 DE DE19620407A patent/DE19620407A1/de not_active Withdrawn
-
1997
- 1997-05-09 US US09/180,862 patent/US6166059A/en not_active Expired - Lifetime
- 1997-05-09 ES ES97923858T patent/ES2205222T3/es not_active Expired - Lifetime
- 1997-05-09 WO PCT/EP1997/002373 patent/WO1997044331A1/de active IP Right Grant
- 1997-05-09 CN CNB97196629XA patent/CN1158267C/zh not_active Expired - Lifetime
- 1997-05-09 BR BR9709107A patent/BR9709107A/pt not_active IP Right Cessation
- 1997-05-09 EP EP97923858A patent/EP0901478B1/de not_active Expired - Lifetime
- 1997-05-09 DE DE59710580T patent/DE59710580D1/de not_active Expired - Lifetime
- 1997-05-09 JP JP54146097A patent/JP4218984B2/ja not_active Expired - Fee Related
- 1997-05-09 AU AU29529/97A patent/AU2952997A/en not_active Abandoned
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102177143A (zh) * | 2008-10-07 | 2011-09-07 | 巴斯夫欧洲公司 | 三唑和咪唑化合物、其应用和含有它们的试剂 |
CN102458124A (zh) * | 2009-06-16 | 2012-05-16 | 巴斯夫欧洲公司 | 杀真菌混合物 |
CN102802416A (zh) * | 2009-06-18 | 2012-11-28 | 巴斯夫欧洲公司 | 杀真菌混合物 |
CN103596934A (zh) * | 2011-05-31 | 2014-02-19 | 株式会社吴羽 | 三氮杂茂化合物、及其运用 |
CN104529918A (zh) * | 2011-05-31 | 2015-04-22 | 株式会社吴羽 | 三氮杂茂化合物、及其运用 |
CN103596934B (zh) * | 2011-05-31 | 2015-08-19 | 株式会社吴羽 | 三氮杂茂化合物、及其运用 |
Also Published As
Publication number | Publication date |
---|---|
JP2000511891A (ja) | 2000-09-12 |
EP0901478A1 (de) | 1999-03-17 |
BR9709107A (pt) | 1999-08-03 |
US6166059A (en) | 2000-12-26 |
EP0901478B1 (de) | 2003-08-13 |
JP4218984B2 (ja) | 2009-02-04 |
CN1158267C (zh) | 2004-07-21 |
AU2952997A (en) | 1997-12-09 |
DE59710580D1 (de) | 2003-09-18 |
WO1997044331A1 (de) | 1997-11-27 |
DE19620407A1 (de) | 1997-11-27 |
ES2205222T3 (es) | 2004-05-01 |
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