Home > Compound List > Product Information
(R)-4-Benzyl-2-oxazolidinone_Molecular_structure_CAS_102029-44-7)
Click picture or here to close

(R)-4-Benzyl-2-oxazolidinone

Catalog No. 13615 Name Sigma Aldrich
CAS Number 102029-44-7 Website http://www.sigmaaldrich.com
M. F. C10H11NO2 Telephone 1-800-521-8956
M. W. 177.19984 Fax
Purity ≥99.5% (sum of enantiomers, GC) Email
Storage Chembase ID: 69958

SYNONYMS

Title
(R)-4-苄基-2-噁唑烷酮
IUPAC name
(4R)-4-benzyl-1,3-oxazolidin-2-one
IUPAC Traditional name
(4R)-4-benzyl-1,3-oxazolidin-2-one

DATABASE IDS

MDL Number MFCD00010846
Beilstein Number 4782551
CAS Number 102029-44-7
PubChem SID 24848261

PROPERTIES

Empirical Formula (Hill Notation) C10H11NO2
Grade puriss.
Purity ≥99.5% (sum of enantiomers, GC)
Melting Point 86-88 °C
Optical Rotation [α]20/D +63±2°, c = 1% in chloroform
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Other Notes
The N-acyl derivatives are used in many enantioselective reactions: aldol reactions with carbonyl compounds. It gives higher yields than other auxiliaries;1 alkylation and Michael reaction;2,3 DA-cycloadditions of 3-acrylates.4
Description (简体中文)
Other Notes
这种 N-芳基衍生物可用于很多对映选择性反应:与羰基化合物的羟醛反应。比使用其他助剂的反应具有更高的产量;1烷基化反应和 Michael 反应;2,3与 3-丙烯酸酯的 DA-环加成反应。4

REFERENCES