(2R,5R)-(+)-2-叔丁基-3-甲基-5-苄基-4-咪唑烷酮

• 产品号: 663093
• CAS号: 390766-89-9
• 分子式: C15H22N2O
• 分子量: 246.34798
• 纯 度: 97%

产品别名

• 标题: (2R,5R)-(+)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone
• IUPAC标准名: (2R,5R)-5-benzyl-2-tert-butyl-3-methylimidazolidin-4-one
• IUPAC传统名: (2R,5R)-5-benzyl-2-tert-butyl-3-methylimidazolidin-4-one
• 别名: (2R,5R)-2-叔丁基-3-甲基-5-苯基甲基-4-咪唑烷酮; (2R,5R)-2-tert-Butyl-3-methyl-5-phenylmethyl-4-imidazolidinone

产品登记号

• CAS号: 390766-89-9
• PubChem SID: 24884184
• MDL号: MFCD08276842

产品性质

• Empirical Formula (Hill Notation): C15H22N2O
• 纯度: 97%
• 熔点: 93-100 °C
• 个人保护装置: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Application
Used in the 1,4-addition of electron-rich benzenes to unsaturated aldehydes, and the asymmetric hydride reduction of α,β-unsaturated aldehydes.1,2
Packaging
1 g in glass bottle
500 mg in glass bottle
Legal Information
U.S. Pat. 6,369,243 and related patents apply. For research purposes only.
Protocols & Applications
Metal-free Asymmetric Catalysis using Macmillan Imidazolidinone Organocatalysts

详细说明 (简体中文)

Application
用于富电子苯的 1,4-加成反应生成不饱和醛，以及 α,β-不饱和醛的不对称氢化物还原反应。1,2
包装
1 g in glass bottle
500 mg in glass bottle
Legal Information
适用美国专利 6,369,243 和相关专利。仅供研究使用。
Protocols & Applications
Metal-free Asymmetric Catalysis using Macmillan Imidazolidinone Organocatalysts