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(2R,5R)-(+)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone_Molecular_structure_CAS_390766-89-9)
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(2R,5R)-(+)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone

Catalog No. 663093 Name Sigma Aldrich
CAS Number 390766-89-9 Website http://www.sigmaaldrich.com
M. F. C15H22N2O Telephone 1-800-521-8956
M. W. 246.34798 Fax
Purity 97% Email
Storage Chembase ID: 140989

SYNONYMS

Title
(2R,5R)-(+)-2-叔丁基-3-甲基-5-苄基-4-咪唑烷酮
IUPAC name
(2R,5R)-5-benzyl-2-tert-butyl-3-methylimidazolidin-4-one
IUPAC Traditional name
(2R,5R)-5-benzyl-2-tert-butyl-3-methylimidazolidin-4-one
Synonyms
(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

DATABASE IDS

CAS Number 390766-89-9
PubChem SID 24884184
MDL Number MFCD08276842

PROPERTIES

Empirical Formula (Hill Notation) C15H22N2O
Purity 97%
Melting Point 93-100 °C
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (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
Description (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

REFERENCES