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Merck
CN

525030

Sigma-Aldrich

邻乙基苯甲醇

98%

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About This Item

线性分子式:
C2H5C6H4CH2OH
CAS号:
分子量:
136.19
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

98%

折射率

n20/D 1.536 (lit.)

沸点

229 °C (lit.)

密度

1.011 g/mL at 25 °C (lit.)

官能团

hydroxyl

SMILES字符串

CCc1ccccc1CO

InChI

1S/C9H12O/c1-2-8-5-3-4-6-9(8)7-10/h3-6,10H,2,7H2,1H3

InChI key

SBUIQTMDIOLKAL-UHFFFAOYSA-N

一般描述

2-Ethylbenzyl alcohol is a benzyl alcohol derivative. Kinetic studies show that the reaction is first-order in both alcohol and oxidant" and forms"corresponding benzaldehydes in acetonitrile and water.

应用

2-Ethylbenzyl alcohol may be used to synthesize 2-ethylbenzyl chloride.

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, multi-purpose combination respirator cartridge (US)


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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访问文档库

Diana Gabriela Vargas-Pineda et al.
Inorganic chemistry, 49(3), 960-968 (2010-01-06)
Organotin(IV) compounds of the type [(o-MeEC(6)H(4))CH(2)](2)SnPh(2-n)Cl(n) were synthesized, E = O, n = 0 (1), n = 1 (2), and n = 2 (3); E = S, n = 0 (4), n = 1 (5), and n = 2 (6);
Oxidation of Benzyl Alcohols with Extraordinarily High Kinetic Isotope Effects.
Jo MR and Seok WK.
Bull. Korean Chem. Soc., 32, 3003-3008 (2011)

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