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Merck

554308

Sigma-Aldrich

2,4,6-三甲基苯乙腈

97%

别名:

2,4,6-三甲基氰苄

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About This Item

线性分子式:
(CH3)3C6H2CH2CN
CAS号:
分子量:
159.23
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

97%

mp

76-80 °C (lit.)

官能团

nitrile

SMILES字符串

Cc1cc(C)c(CC#N)c(C)c1

InChI

1S/C11H13N/c1-8-6-9(2)11(4-5-12)10(3)7-8/h6-7H,4H2,1-3H3

InChI key

SDKQOGSGNPGPRN-UHFFFAOYSA-N

一般描述

2,4,6-Trimethylphenylacetonitrile is formed as an intermediate during the synthesis of mesitylacetic acid.[1]

应用

2,4,6-Trimethylphenylacetonitrile (Mesitylacetonitrile) may be used in the preparation of 2,4,6-trimethyl-,9-phenethylamine hydrochloride.[2] It may also be employed in the synthesis of the following compounds:[3]
  • ethyl mesitylacetate
  • α-mesitylacetoacetonitrile
  • mesitylacetone
  • β-hydroxy-a-mesitylacrylonitrile
  • α-mesitylpropionic acid
  • α-mesityl-8-phenylpropionitrile

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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

A synthesis of α-mesitylpropiomesitylene.
Fuson RC, et al.
The Journal of Organic Chemistry, 9(2), 187-192 (1944)
Mescaline analogs. Iii. 2, 4, 6-trialkyl-and 3, 4-dihydroxy-5-methoxy-β-phenethylamines.
Benington F, et al.
The Journal of Organic Chemistry, 20(9), 187-192 (1944)
Mesitylacetic acid.
Fuson RC and Rabjohn N.
Organic Syntheses, 69-69 (1955)

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