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(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride_Molecular_structure_CAS_278173-23-2)
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(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride

Catalog No. 569763 Name Sigma Aldrich
CAS Number 278173-23-2 Website http://www.sigmaaldrich.com
M. F. C13H19ClN2O Telephone 1-800-521-8956
M. W. 254.75576 Fax
Purity 97% Email
Storage Chembase ID: 145038

SYNONYMS

Title
(5S)-(-)-2,2,3-三甲基-5-苄基-4-咪唑啉酮 单盐酸盐
IUPAC name
(5S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride
IUPAC Traditional name
(5S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride

DATABASE IDS

MDL Number MFCD03426983
CAS Number 278173-23-2
PubChem SID 24880521

PROPERTIES

Empirical Formula (Hill Notation) C13H18N2O · HCl
Purity 97%
Melting Point 157-161 °C(lit.)
Optical Rotation [α]20/D -67°, c = 1 in H2O
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
Metal-free OrganoCatalyst technology for asymmetric catalysis. Catalyzes asymmetric Diels-Alder reactions, 1,3-dipolar additions and pyrrole alkylations in high enantiomeric excess.1,2,3
Used in first highly enantioselective organocatalytic Diels-Alder reaction and 1,3-dipolar addition.
Packaging
2 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
用于不对称催化反应的无金属 OrganoCatalyst 技术。以高对映体过剩率催化不对称 Diels-Alder 反应、1,3-偶极加成反应和吡咯烷基化反应。1,2,3
用于首例高对映选择性有机催化 Diels-Alder 反应和 1,3-偶极加成。
包装
2 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