所有图片(1)
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
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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
警示用语：
Warning
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
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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