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Merck

349712

Sigma-Aldrich

氯乙酸苄酯

99%

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About This Item

线性分子式:
ClCH2CO2CH2C6H5
CAS号:
分子量:
184.62
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

方案

99%

折射率

n20/D 1.525 (lit.)

沸点

90 °C/1 mmHg (lit.)

密度

1.215 g/mL at 25 °C (lit.)

官能团

chloro
ester
phenyl

SMILES字符串

ClCC(=O)OCc1ccccc1

InChI

1S/C9H9ClO2/c10-6-9(11)12-7-8-4-2-1-3-5-8/h1-5H,6-7H2

InChI key

SOGXBRHOWDEKQB-UHFFFAOYSA-N

一般描述

Benzyl chloroacetate is an ester.

应用

Benzyl chloroacetate may be used:
  • in the synthesis of monoesters of phosphonoacetic acid
  • in the synthesis of N-benzoyl-glycyl- hydroxyl acetic acid, ester substrate for carboxypeptidase Y catalyzed peptide synthesis
  • as reagent in the total syntheses of the (±)-di-O-methyl ethers of the norlignans sequirin-A, agatharesinol, and hinokiresinol, and of (±)-tri-O-methyl sequirin-E

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Influence of the substrate structure on carboxypeptidase Y catalyzed peptide bond formation.
Breddam K, et al.
Carlsberg Research Communications, 45(5), 361-367 (1980)
T R Herrin et al.
Journal of medicinal chemistry, 20(5), 660-663 (1977-05-01)
The synthesis of monoesters (P and C) of phosphonoacetic acid (PA) is given. The carboxyl esters were prepared by two methods: the reaction of chloroacetates with tris(trimethylsilyl) phosphite, followed by hydrolysis; and by the acid-catalyzed esterification of PA with the
Stereoselective total syntheses of the (?)-di-O-methyl ethers of agatharesinol, sesquirin-A, and hinokiresinol, and of (?)-tri-O-methylsequirin-E, characteristic norlignans of coniferae.
Beracierta AP and Whiting DA.
Journal of the Chemical Society. Perkin Transactions 1, 10, 1257-1263 (1978)

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