CAS: 121552-61-2; Cyprodinil

欧盟法规

[ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号21573-10-4 环丙基-1,3-丁二酮 | CAS号6685-76-3 苯基胍碳酸盐

环丙甲酰丙酮,苯基胍碳酸盐 以 乙醚,水 用作溶剂,以74.5%的收率获得嘧菌环胺
参考文献:Pesticides
标题:Pesticides
摘要:公式为##str1##的化合物,其中:R.Sub.1和r.Sub.2彼此独立地是氢,卤素,C.Sub.1-C.Sub.3烷基,C.Sub.1-C.Sub.2卤代烷基,C.Sub.1-C.Sub.3烷氧基或c.Sub.1-C.Sub.3卤代烷氧基;R.Sub.3是氢;C.Sub.1-C.Sub.4烷基;或由卤素,羟基或氰基取代的c.Sub.1-C.Sub.4烷基;环丙基;或由甲基和/或卤素单取代至三取代的环丙基;以及r.Sub.4是c.Sub.3-C.Sub.6环烷基或由甲基和/或卤素单取代至三取代的c.Sub.3-C.Sub.6环烷基,具有有价值的杀菌和杀虫性能.这种新型活性成分可用于植物保护,用于防止植物病原微生物或有害昆虫对栽培植物的侵害,并用于控制这些害虫.

专利信息

专利号:WO-2022146324-A1
优先权日:2020-12-29
标 题 :Synthesis of pyrimidine-4(lh)-one derivatives from new hydrazineylidene
发明人：SARIPINAR EMIN; BURCU HILAL JANSET; KEKEÇMUHAMMED HÃœSEYIN; TAPERA MICHAEL
权利人:T C ERCIYES UENIVERSITESI
摘要:This invention relates to the synthesis of pyrimidine-4 (1H)-one derivatives from Meldrum's acid, carbonyl compounds (aldehyde/ketone), and guanylhydrazone derivatives and tautomers, enantiomers, and salts thereof.

专利号:US-5900568-A
优先权日:1998-05-15
标题:Method for automatic sound synthesis
发明人：ABRAMS STEVEN R
权利人:IBM
摘要:A method for automatically adjusting the parameters of a synthesizer includes generating a first synthesized signal based on an initial set of synthesizer parameters, comparing the first synthesized signal to an input sound signal, and generating a control signal for adjusting a subset of parameters of the synthesizer to minimize the differences between the first synthesized signal and the input sound signal. These steps may be iteratively performed for a predetermined number of additional subsets of synthesizer parameters, until a final output of the synthesizer is obtained which represents an optimization of the synthesis of the input sound signal.

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-2013290818-A1
优先权日:2012-04-27
标 题:Method and apparatus for switching between presentations of two media items
发明人：ARRASVUORI JUHA HENRIK; ERONEN ANTTI JOHANNES; LEHTINIEMI ARTO JUHANI
权利人:ARRASVUORI JUHA HENRIK; ERONEN ANTTI JOHANNES; LEHTINIEMI ARTO JUHANI; NOKIA CORP
摘要:An approach is provided for switching between presentations of two media items. A media platform determines a request to cause, at least in part, a switching of a presentation of a first media item to a second media item. The media platform processes and/or facilitates a processing of metadata associated with the first media item, the second media item, or a combination thereof to cause, at least in part, a synthesis of one or more transitions. The media platform causes, at least in part, a presentation of the one or more transitions during the switching.

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).