CAS: 24066-82-8; Ethyl 2-Isothiocyanatoacetate

该化合物是一种有机化合物,其特征为异硫代亚胺化合物功能组和酯组,该化合物一般是无色的,淡黄色的,有独特气味的液体,在乙醇和乙醚等有机溶剂中溶解,但在水中溶解性有限.乙酰2-异硫代亚代亚代亚酸酯因其活性而闻名,特别是在核糖代用品反应中,由于异硫代亚酸物组的电动力性质,该化合物经常用于有机合成,可用作各种化学反应的建筑块,包括硫柳亚胺和其他含氮化合物的合成.此外,该化合物可能展示生物活动,使其对医药化学和农用化学应用具有兴趣.许多异硫氰酸,因此必须谨慎处理该化合物,因为潜在毒性和刺激性.

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合成工艺路线路线简述

  • 合成目标产物 Ethyl Isothiocyanatoacetate 主要起始原料 Carbon Disulfide And Glycine Ethyl Ester Hydrochloride
  • (文献来源)合成步骤主要原料 Carbon Disulfide 和 Glycine Ethyl Ester Hydrochloride
异氰基乙酸乙酯置于mo(O)(S2Cnet2)2 硫化丙烯体系中,用 二氯甲烷 用作溶剂,化学反应 72.0H,以87%的收率获得异硫氰基乙酸乙酯
参考文献:Direct Synthesis Of Isothiocyanates From Isonitriles By Molybdenum-Catalyzed Sulfur Transfer With Elemental Sulfur
标题:Direct Synthesis Of Isothiocyanates From Isonitriles By Molybdenum-Catalyzed Sulfur Transfer With Elemental Sulfur
摘要:The Direct Molybdenum-Catalyzed Sulfuration Of A Variety Of Isonitriles With Elemental Sulfur Or Propene Sulfide As Sulfur Donors Affords The Corresponding Isothiocyanates In Good Yields And Under Mild Reaction Conditions. A Catalytic Cycle Is Suggested,In Which The Molybdenum Oxo Disulfur Complex Operates As The Active Sulfur-Transferring Species. A Novel Adduct Between The Isonitrile And The Molybdenum Complex Has Been Characterized By X-Ray Analysis And Its Association Constant Determined By Uv-Vis Spectroscopy,But This Adduct Appears Not To Be Involved In The Sulfur-Transfer Process.
Doi:10.1021/jo026042I

海关参考信息

专利信息


专利号:US-2011166152-A1
优先权日:2008-10-02
标题 :Heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase
发明人:LECLERC JEAN-PHILIPPE; LI CHUN SING; RAMTOHUL YEEMAN K
权利人:LECLERC JEAN-PHILIPPE; LI CHUN SING; RAMTOHUL YEEMAN K
摘要:Heteroaromatic compounds of structural formula (I) are inhibitors of stearoyl-coenzyme A delta-9 desaturase (SCD). The compounds of the present invention are useful for the prevention and treatment of conditions related to abnormal lipid synthesis and metabolism, including cardiovascular disease, such as atherosclerosis; obesity; Type 2 diabetes; insulin resistance; hyperglycemia; Metabolic Syndrome; neurological disease; cancer; and liver steatosis.

专利号:US-2010197692-A1
优先权日:2007-07-20
标 题 :Bicyclic heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase
发明人:RAMTOHUL YEEMAN K; LI CHUN SING; LECLERC JEAN-PHILIPPE
权利人:MERCK FROSST CANADA LTD
摘要:Bicyclic heteroaromatic compounds of structural formula I are inhibitors of stearoyl-coenzyme A delta-9 desaturase (SCD). The compounds of the present invention are useful for the prevention and treatment of conditions related to abnormal lipid synthesis and metabolism, including cardiovascular disease; atherosclerosis; obesity; diabetes; neurological disease; metabolic syndrome; insulin resistance; liver steatosis; and non-alcoholic steatohepatitis.

专利号:WO-9213530-A1
优先权日:1991-02-11
标题 :Transglutaminase enzyme inhibitors
发明人:CHEN GEORGE T
权利人:MEDICIS CORP
摘要:The present invention relates to a composition and method for regulating protein crosslinking by transglutaminase enzymes in an animal or human. More particularly, the present invention relates to a series of novel transglutaminase enzyme inhibitors having the general formula: R-C=O-(CH2)n-NCS, wherein R is selected from the group consisting of O-CH3, O-CH2-CH3, O-Ø, O-Bz, and NH2 and n is an integer between 1 and 4, to their synthesis, and to their use in the treatment of crosslinking and amine incorporation disorders.
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合成参考文献


摘要:Aitken, R. A., Science of Synthesis Knowledge Updates, (2018) 3, 337.
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