相似化合物
4333-20-4 2010-15-3 7390-20-7欧盟法规
ECHA物质C&L通报REACH预注册上下游产品
CAS号701-73-5 METHYL DITHI°CA... | CAS号302-72-7 DL-2-氨基丙酸 | CAS号103-72-0 异硫氰酸苯酯 | CAS号104892-42-4 N-phenylthi°Car... | CAS号17344-99-9 2-amino-propion... | CAS号75-15-0 二硫化碳 | CAS号74-88-4 碘甲烷 | CAS号7783-06-4 硫化氢 | CAS号302-72-7 DL-2-氨基丙酸合成工艺路线路线简述
- 合成目标产物 Phenylthiohydantoin-Dl-Alanine 主要起始原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
- (文献来源)合成步骤主要原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
📜N-Phenylthiocarbamoyl-Dl-Alanine置于盐酸体系中,用 1,4-二氧六环,水 作为反应溶剂,化学反应 0.03H,以1.34 G的收率获得产物苯基硫代乙内酰脲-丙氨酸
参考文献:氨基脲脱水环化微波辅助合成1,3,4-恶二唑/硫代乙内酰脲杂化衍生物
标题:氨基脲脱水环化微波辅助合成1,3,4-恶二唑/硫代乙内酰脲杂化衍生物
摘要:E-Mail: Ydgong@dongguk.Edu 2014 年 7 月 29 日收到,2014 年 9 月 16 日接受 合成了一系列含有 1,3,4-恶二唑和硫代乙内酰脲的化合物,作为一种有前途的药物化学支架.合成的关键步骤是使用 Pocl 对在一个酰基末端具有硫代乙内酰脲部分的氨基脲进行微波辅助环化
DOI:10.5012/bkcs.2014.35.12.3609
海关参考信息
- 2912110000-甲醛
2912120000-乙醛
2921211000-乙二胺
2924199090-其他无环酰胺 - 💡 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
专利信息
专利号:US-6090250-A
优先权日:1993-09-20
标题 :Chiral surfactants and methods for their use in chiral separations
发明人:MAZZEO JEFFREY R; GROVER EDWARD R; SWARTZ MICHAEL E; MERION MICHAEL; PETERSEN JOHN S
权利人:WATERS INVESTMENTS LTD
摘要:PCT No. PCT/US94/10655 Sec. 371 Date Mar. 20, 1996 Sec. 102(e) Date Mar. 20, 1996 PCT Filed Sep. 20, 1994 PCT Pub. No. WO95/08529 PCT Pub. Date Mar. 30, 1995Chiral surfactants, methods for their synthesis and use, and apparatus designed to facilitate chiral separations using nucellar capillary electrophoresis is disclosed. A chiral surfactant having the general formula: is described, R1 is the hydrophobic tail, Y-A-X is the linker, the brackets define a chiral center, and the hydrophilic head group is Z. All the various components may potentiate the enantioselectivity of the chiral surfactant. The capillary electrophoresis (CE) system includes a narrow diameter capillary, a high voltage power supply, an electrolyte reservoir at each end of the capillary, a means for injecting a sample, and a detector. Chiral surfactants are dissolved in the electrolyte above their critical micelle concentration (cmc), resulting in the formation of chiral micelles. The electrolyte reservoirs and capillary tube are filled with the electrolyte. A sample containing a mixture of enantiomers is then injected into the capillary, and a high voltage potential is applied across the capillary. The sample components migrate through the capillary due to the influence of the applied electric field. An example separation of the four sereoisomers of aspartame is shown.