CAS: 746657-36-3; (1R,2S)-Ethyl 1-Amino-2-Vinylcyclopropanecarboxylate
- 英文名称(1R,2S)-Ethyl 1-Amino-2-Vinylcyclopropanecarboxylate
- 中文名称(1R,2S)-1-氨基-2-乙烯基环丙烷羧酸乙酯
- IUPAC名称ethyl (1R,2S)-1-amino-2-vinylcyclopropane-1-carboxylate
- 其它别名(1R,2S)-1-氨基-2-乙烯-环丙烷羧酸乙酯; Ethyl(1R,2S)-1-Amino-2-Vinylcyclopropane-1-Carboxylate
- CAS编号746657-36-3
- MFCD编号:MFCD11042407
- 分子式:C8H13NO2分子量:155.2
- 产品CID: 1737316
- 产品分类有机原料→分子砌块→脂肪环类化合物→环丙烷类化合物
相似化合物
213316-49-5 681807-59-0 259217-95-3物理性质
MSDS等安全信息
上下游产品
(trans)-ethyl 1-amino-2-vinylcyclopropanecarboxylate hydr°Chloride rac-(1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid ethyl ester N-B°C-(1R,2S)-1-amino-2-vinylcyclopropane carboxylic acid ethyl ester (1R,2S)/(1S,2R) 1-amino-2-vinylcyclopropane carboxylic acid ethyl ester(2S,4R)-2-((1R,2S)-1-ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester ethyl (1R,2S)-1-({(4S)-1-[(2S)-2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-8-nonenoyl]-4-hydroxy-L-prolyl}amino)-2-ethenylcyclopropanecarboxylate (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid t-butyl ester (1R,2S)-1-(9H-fluoren-9-ylmethoxycarbonylamino)-2-vinylcyclopropanecarboxylic acid合成工艺路线路线简述
📜1-叔丁氧羰基氨基-2-乙烯基环丙烷甲酸乙酯置于盐酸,Ammonium Hydroxide,二氧化碳体系中,用 1,4-二氧六环,乙酸乙酯 作为反应溶剂,化学反应 3.0H,反应生成 (1R,2S)-1-氨基-2-乙烯-环丙烷羧酸乙酯
参考文献: Calpain Modulators And Methods Of Production And Use Thereof[fr] Modulateurs De Calpaïne Et Leurs Méthodes De Production Et D'Utilisation
标题: Calpain Modulators And Methods Of Production And Use Thereof[fr] Modulateurs De Calpaïne Et Leurs Méthodes De Production Et D'Utilisation
摘要:这项技术涉及到用于治疗纤维化疾病的化合物,试剂盒,组合物和方法.在某些方面,这项技术提供了治疗与卡尔帕因(如capn1,Capn2和/或capn9)至少部分相关或介导的各种疾病或疾病的方法.这项技术通常适用于抑制肌成纤维细胞分化的化合物.
海关参考信息
- 2901210000-乙烯
2901220000-丙烯
2905121000-正丙醇
2909110000-乙醚 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:A Concise Synthesis Of The Hcv Protease Inhibitor Biln 2061 And Its P3 Modified Analogs作者:Dejun Liu,Jingchao Dong,Yunxing Yin,Rujian Ma,Yifeng Shi,Hao Wu,Shuhui Chen,Ge Li |发布日期:2011.7
摘要:A Concise Synthesis Of Biln 2061 Was Achieved Through More Efficient Installation Of P2 4‐quinoline Moiety Via Sn2 Displacement Of The β‐obs Group Located On The 4‐hydroxyl Proline Intermediate, Which Was Prepared From 4‐α‐hydroxyl Proline Analog Via Mitsunobu Reaction With Inversion Of Stereochemistry. In Addition, A Short And Practical Synthesis For P3 Unit Is Also Described Herein. Final Assembly
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