CAS: 78587-05-0; (S,S)-Hexythiazox

欧盟法规

[欧盟农药活性物质

上下游产品

trans-4-methyl-5-(4-chlorophenyl)-2-thiazolidone Cyclohexyl is°Cyanate 4'-chloropropiophenone 1-(4-chlorophenyl)-2-(hydroxyimino)propan-1-one

Trans-4-Methyl-5-(4-Chlorophenyl)-2-Thiazolidone,环己基异氰酸酯 以 二甲基亚砜作为反应溶剂,获得 Hexythiazox
参考文献:Heteroyclic Compounds
标题:Heteroyclic Compounds
摘要:一种化合物的分子式为##str1##其中x,Y和z的典型表示形式为氧或硫;R.Sub.1为甲基;R.Sub.2为苯基,取代基为氯,甲基,甲氧基,硝基或亚甲氧基;R.Sub.3为环己基,甲基环己基或四氢吡喃基,可用作杀螨剂.

专利信息

专利号:US-10423780-B1
优先权日:2016-08-04
标 题 :System and method for synthesis of correct-by-construction cryptographic software from specification
发明人：KOPYLOV ALEXEI; NOGIN ALEKSEY
权利人:HRL LAB LLC
摘要:Described is a system for synthesis of cryptographic software from specification. During operation, the system generates a first level formalization code of a cryptographic protocol based on a user input protocol specification and a library of transformation rules. A second level formalization code is then generated by implementing communication protocols to the first level formalization code. A third level formalization code subsequently generated by implementing cryptographic primitives to the second level formalization code. Finally, the third level formalization code is encoded on a computer readable medium as an executable code.

专利号:EP-1397373-B1
优先权日:2001-06-07
标 题 :Improved synthesis of allofuranose
发明人：KOCH TROELS; HANSEN HENRIK FRYDENLUND
权利人:SANTARIS PHARMA AS
摘要:The present invention provides a novel strategy for the synthesis of allofuranose using glucofuranose as starting material in a one-pot reaction. The novel finding is that it is possible to carry out the oxidation of 1,2: 5,6-di-O-isopropylidene- alpha -D-glucofuranose with DMSO/acetic anhydride and a reduction reaction in one pot obtaining high yields of recrystallised and analytical pure 1,2:5,6-di-O-isopropylidene- alpha -D-allofuranose.

专利号:US-6858726-B2
优先权日:2001-06-07
标 题:Synthesis of allofuranose
发明人：KOCH TROELS; HANSEN HENRIK FRYDENLUND
权利人:SANTARIS PHARMA AS
摘要:The present invention provides a novel strategy for the synthesis of allofuranose using glucofuranose as starting material in a one-pot reaction. The novel finding is that it is possible to carry out the oxidation of 1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose with DMSO/acetic anhydride and a reduction reaction in one pot obtaining high yields of recrystallised and analytical pure 1,2:5,6-di-O-isopropylidene-alpha-D-allofuranose.

专利号:WO-2025056767-A1
优先权日:2023-09-15
标题 :Process for the preparation of enantiomerically enriched aliphatic amines
发明人：BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS
权利人:SYNGENTA CROP PROTECTION AG
摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.

专利号:US-2016073631-A1
优先权日:2013-03-04
标 题 :Process for the preparation of dihydropyrrole derivatives
发明人：EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS
权利人:SYNGENTA PARTICIPATIONS AG; SYNGENTA LTD
摘要:The present invention provides stereoselective processes for the preparation of compounds of formula (I) n n n n n n n n n n n n wherein n P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; n R 1 is chlorodifluoromethyl or trifluoromethyl; n R 2 is optionally substituted aryl or optionally substituted heteroaryl; n n is 0 or 1; n including the process comprising n (a-i) reacting a compound of formula II n n n n n n n n n n n n n n n n wherein P, R 1 and R 2 are as defined for the compound of formula I; n with nitromethane in the presence a chiral catalyst to give a compound of formula III n n n n n n n n n n n n n n n n wherein P, R 1 and R 2 are as defined for the compound of formula I; and n (a-ii) reductively cyclising the compound of formula III to give the compound of formula I. n n n n n The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).

专利号:US-9233920-B2
优先权日:2010-06-11
标题 :Process for the preparation of dihydropyrrole derivatives
发明人：EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS
权利人:EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS; SYNGENTA PARTICIPATIONS AG; SYNGENTA LTD
摘要:The present invention provides stereoselective processes for the preparation of compounds of formula (I) wherein P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; R 1 is chlorodifluoromethyl or trifluoromethyl; R 2 is optionally substituted aryl or optionally substituted heteroaryl; n is 0 or 1; including the process comprising (a-i) reacting a compound of formula II wherein P, R 1 and R 2 are as defined for the compound of formula I; with nitromethane in the presence a chiral catalyst to give a compound of formula III Wherein P, R 1 and R 2 are as defined for the compound of formula I; and (a-ii) reductively cyclizing the compound of formula III to give the compound of formula I. The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).