744298
(5R)-5-(1H-Indol-3-ylmethyl)-2,2,3-trimethyl-4-imidazolidinone monohydrochloride
≥98.5% (HPLC)
登录查看公司和协议定价
选择尺寸
关于此项目
经验公式（希尔记法）:
C15H19N3O · HCl
化学文摘社编号:
分子量:
293.79
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
方案
≥98.5% (HPLC)
98.5-101.5% (AT)
表单
solid
旋光性
[α]/D +106 to +105°, c = 1.43 in methanol
适用性
conforms to structure for Infrared spectrum
SMILES字符串
Cl.CN1C(=O)[C@@H](Cc2c[nH]c3ccccc23)NC1(C)C
InChI
1S/C15H19N3O.ClH/c1-15(2)17-13(14(19)18(15)3)8-10-9-16-12-7-5-4-6-11(10)12;/h4-7,9,13,16-17H,8H2,1-3H3;1H/t13-;/m1./s1
InChI key
YYTZVVHQTSYLLZ-BTQNPOSSSA-N
应用
Organocatalyst for highly enantioselective Diels-Alder reactions.
法律信息
U.S. Pat. 6,369,243 and related patents apply. For research purposes only.
Guilong Li et al.
Angewandte Chemie (International ed. in English), 52(17), 4628-4632 (2013-03-23)
Mild Magic: A mild, enantioselective Diels-Alder reaction, catalyzed by a chiral magnesium phosphate species, has been developed for the synthesis of various chiral spirooxindoles. Molecular sieves were found to have a considerable effect when used as additives in this reaction.
Asymmetric Intramolecular Aza?Michael Reaction Using Environmentally Friendly Organocatalysis.
Takasu, K., et al.
Heterocycles, 59, 51-55 (2003)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持