CAS: 23564-06-9; Thiophanat-Ethyl

相似化合物

27079-29-4 412912-51-7 949791-69-9

上下游产品

1,2-diamino-benzene Ethoxycarbonyl isothi°Cyanate

📜邻苯二胺,异硫氰酰甲酸乙酯置于四甲基乙二胺体系中,用 乙酸乙酯 用作溶剂,化学反应 5.0H,反应生成硫菌灵
参考文献:Tmeda催化合成n-芳基-N'-乙氧基羰基硫脲和芳烃(或聚亚甲基)-双-乙氧基羰基硫脲衍生物
标题:Tmeda催化合成n-芳基-N'-乙氧基羰基硫脲和芳烃(或聚亚甲基)-双-乙氧基羰基硫脲衍生物
摘要:报道了一种由 Tmeda 催化合成乙氧羰基异硫氰酸酯和乙氧羰基硫脲的新方法.通过该方法在室温下合成了一系列n-芳基-N'-乙氧基羰基硫脲和芳烃(或聚亚甲基)-双-乙氧基羰基硫脲衍生物,产率从非常好到优异.
Doi:10.1080/10426500490474905

专利信息

专利号:EP-1578714-B1
优先权日:2002-12-20
标题:Novel chiral compounds derived from hexanoic acid esters, method and intermediate chemicals for the preparation and use thereof for synthesis of 2-(bromomethyl)2-ethyl hexanoic chiral acid
发明人：CROCQ-STUERGA VERONIQUE; ROUSSEL PATRICK
权利人:AVENTIS PHARMA SA
摘要:The invention relates to a chiral compound of a formula (I), wherein R1 is hydroxyl or a carboxy activator group and R2 is alkyl eventually substituted by halogen or benzyl. The preparation and the use of the inventive compound for synthesis of 2-bromomethyl-2-ethyl hexanoic chiral acid and the novel intermediate chemicals are also disclosed.

专利号:WO-9214492-A1
优先权日:1991-02-14
标 题:In situ synthesis of radiopharmaceuticals
发明人：VERBRUGGEN ALFONS M
权利人:MALLINCKRODT MEDICAL INC
摘要:The present invention relates to a process of making radiopharmaceuticals in situ, i.e. wherein a radionuclide and an acyclic ligand react with constituents of the complex forming reaction solution to produce an administratable radiopharmaceutical agent. By forming radiopharmarceuticals according to the present invention, it is possible to obtain radiopharmaceuticals previously unattainable because of problems associated with the ligand synthesis or with the complex forming reaction.

专利号:US-5350681-A
优先权日:1986-08-18
标题 :Enzymatic membrane method for the synthesis and separation of peptides
发明人：IACOBUCCI GUILLERMO A; BROSE DANIEL J; RAY RODERICK J; VAN EIKEREN PAUL
权利人:COCA COLA CO
摘要:The present invention discloses a method for the enzymatic synthesis of a peptide. A protected peptide having a C-terminal carboxylate group or a protected, N-acyl amino acid having an alpha carboxylate group is reacted with a protected peptide having an N-terminal ammonium group or a protected amino acid having an alpha ammonium group in the presence of a condensation enzyme under conditions in which the carboxylate group and the ammonium group condense to form a protected, uncharged, peptide product. This peptide product is transported across a water-immiscible hydrophobic phase into an aqueous product phase and prevented from back diffusing across the water-immiscible hydrophobic phase. The peptide product can be converted, chemically or enzymatically, to a charged species that cannot back diffuse across the water-immiscible phase into the aqueous reaction phase. The water-immiscible hydrophobic phase is an ion rejection membrane separating the aqueous reaction phase from the product phase creating oil/water interfaces with each of the aqueous phases.

专利号:US-9951149-B2
优先权日:2013-06-17
标 题 :Reversible heparin molecules and methods of making and using the same
发明人：LIU JIAN; XU YONGMEI; LINHARDT ROBERT J; HARRIS EDWARD
权利人:UNIV NORTH CAROLINA CHAPEL HILL; RENSSELAER POLYTECH INST; NUTECH VENTURES; RENSSELAER POLYECHNIC INST
摘要:Methods and systems for synthesizing heparin compounds are provided. The chemoenzymatic synthesis of structurally homogeneous low molecular weight heparins that have a reversible anticoagulant activity is provided. Also disclosed are heparin compounds having anticoagulant activity, including a binding affinity to antithrombin and an anti-Xa activity, but no detectable anti-lla activity. Additionally, provided are synthetic, low-molecular weight heparin compounds with reversible anticoagulant activity, where the anticoagulant activity is reversible by protamine.

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-4246373-A
优先权日:1980-02-14
标 题 :Synthesis of substituted cyclopentadienes and cyclopentadiene-functionalized polymers
发明人：KENNEDY JOSEPH P; CASTNER KENNETH F
权利人:KENNEDY JOSEPH P; CASTNER KENNETH F
摘要:Aluminum cyclopentadienyl compounds can be used to synthesize a variety of organic molecules containing the cyclopentadiene group, e.g., substituted cyclopentadiene compounds, polymer molecules with cyclopentadiene pendant groups, and polymer molecules with cyclopentadiene terminal groups.