CAS: 88621-01-6; 7-{2-[(2-Aminothiazol)-4-Yl]-2-[(Z)(Methoxycarbonyl)Methoxyimino]Acetamido}-3-Vinyl-Ceph-3-Em-4-Carboxylic Acid

英文名称7-{2-[(2-Aminothiazol)-4-Yl]-2-[(Z)(Methoxycarbonyl)Methoxyimino]Acetamido}-3-Vinyl-Ceph-3-Em-4-Carboxylic Acid
中文名称头孢克肟甲酯
CAS编号88621-01-6
分子式:C17H17N5O7S2分子量:467.48
产品CID: 1901030
产品分类化学试剂 → 有机试剂 → 肟

相似结构搜索
InChIKey: ZDPJGEMACCCYJO-QVJRADPESA-N
ZDPJGEMACCCYJO-QVJRADPESA-N
计算化学: 氢键受体数12.0氢键供体数3.0可旋转键数9.0

MSDS等安全信息

警示词warning
危险描述H303 May be harmful if swallowed+H313 Skin contact may be harmful+H333 Inhalation may be harmful to the body
防范说明P264+P280+P305+P351+P338+P337+P313
安全声明H303+H313+H333

上下游产品

7-氨基-3-乙烯基-3-头孢环-4-羧酸 7-Avca 79349-82-9

合成工艺路线路线简述

246035-38-1 + 79349-82-9 = 88621-01-6
反应条件:1.1 Reagents: Triethylamine Solvents: Ethyl Acetate,Water; 4 H,10 - 15 °C1.2 Reagents: Hydrochloric Acid Solvents: Water; Ph 7.5 - 8,10 - 15 °C1.3 Reagents: Hydrochloric Acid Solvents: Water; Ph 1.4 - 1.6,10 - 15 °C; 1 H,10 - 15 °C; 15 °C -> 5 °C; 1 H,0 - 5 °C
标题:Synthesis Of Cefixime
作者:Chen,Xin; Wang,Chen-Zhu; Zhang,Min
参考文献:Zhongguo Kangshengsu Zazhi 日期:2012 卷标:37(9) 页码:687-690

📜7-{2-[(2-Aminothiazol)-4-Yl]-2-[(Z)(Methoxycarbonyl)Methoxyimino]Acetamido}-3-Vinyl-Ceph-3-Em-4-Carboxylic Acid Tert.octylamine Salt置于sodium Hydroxide,盐酸,D-异抗坏血酸体系中,用水作为反应溶剂,化学反应生成头孢克肟甲酯
参考文献:Process For Purification Of A Cephalosporin Derivative
标题:Process For Purification Of A Cephalosporin Derivative
摘要:一种通过新型叔辛基胺盐的头孢克肟中间体纯化的方法,该中间体可能是晶体,可以通过从7-氨基-3-乙烯基头孢-3-酯-4-羧酸一锅反应中制备.