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Merck
CN

459860

Sigma-Aldrich

顺式-1,3-O-苄烯丙三醇

97%

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别名:
2-苯基-1,3-二噁唑-5-醇
经验公式(希尔记法):
C10H12O3
CAS号:
分子量:
180.20
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

形式

solid

mp

83-86 °C (lit.)

储存温度

2-8°C

SMILES字符串

O[C@@H]1CO[C@@H](OC1)c2ccccc2

InChI

1S/C10H12O3/c11-9-6-12-10(13-7-9)8-4-2-1-3-5-8/h1-5,9-11H,6-7H2/t9-,10+

InChI key

BWKDAAFSXYPQOS-AOOOYVTPSA-N

一般描述

cis-1,3-O-Benzylideneglycerol participates as a monomer in the preparation of novel oligomeric prepolymers. cis-derivatives are obtained from the acylation and etherification of cis-1,3-O-benzylideneglycerol.

应用

Reactant involved in synthesis of biologically active molecules including:
  • Arachidonoylglycerol mimetics selective for CB1 receptors
  • Core disaccharides from Streptococcus pneumoniae type 23F capsular polysaccharide antigen†
  • Anionic demdrimers for use as antibacterial agents

Reactant involved in synthesis of:
  • Isoglycerol methacrylate-lactide amphiphilic block copolymers and supramolecular aggregates
  • Hyperbranched polyalkenamer-polyesters via acyclic diene metathesis polymerization
  • Protected branched glycerol oligomer

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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520. Aspects of stereochemistry. Part IV. Configuration and some reactions of the 1, 3-O-benzylideneglycerols (5-hydroxy-2-phenyl-1, 3-dioxans).
Baggett N, et al.
Journal of the Chemical Society, 2574-2581 (1960)
Synthesis of hyperbranched P poly (glycerol-diacid) oligomers.
Wyatt VT, et al.
Journal of the American Oil Chemists' Society, 83(12), 1033-1039 (2006)

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