跳转至内容
Merck
CN

527726

4-乙基苯甲腈

98%

登录 查看组织和合同定价。

选择尺寸


关于此项目

线性分子式:
C2H5C6H4CN
化学文摘社编号:
分子量:
131.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
246-811-5
MDL number:
Assay:
98%
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

InChI key

SXFFMFAQNAFSLF-UHFFFAOYSA-N

InChI

1S/C9H9N/c1-2-8-3-5-9(7-10)6-4-8/h3-6H,2H2,1H3

SMILES string

CCc1ccc(cc1)C#N

assay

98%

refractive index

n20/D 1.527 (lit.)

bp

237 °C (lit.)

density

0.956 g/mL at 25 °C (lit.)

functional group

nitrile

General description

4-Ethylbenzonitrile is an electron deficient aromatic nitrile.

Application

4-Ethylbenzonitrile may be used in the preparation of:
  • 2-(3-bromo-phenyl)-4,6-bis-(4-ethyl-phenyl)-[1,3,5]-triazine
  • mixture of 1-benzyl-2-methylbenzene and 1-benzyl-4-methylbenzene

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

208.0 °F - closed cup

flash_point_c

97.8 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Antonio Herrera et al.
The Journal of organic chemistry, 79(15), 7012-7024 (2014-07-11)
The reaction of equimolecular amounts of a nitrile and triflic anhydride or triflic acid at low temperature produces an intermediate nitrilium salt that subsequently reacts with 2 equiv of a different nitrile at higher temperature to form 2,4-disusbstituted-6-substituted 1,3,5-triazines in
Polystyrene Backbone Polymers Consisting of Alkyl-Substituted Triazine Side Groups for Phosphorescent OLEDs.
Salert BCD, et al.
Advances in Materials Science and Engineering (2012)
Ji-Bao Xia et al.
Journal of the American Chemical Society, 135(46), 17494-17500 (2013-11-05)
We report herein an operationally simple method for the direct conversion of benzylic C-H groups to C-F. We show that visible light can activate diarylketones to abstract a benzylic hydrogen atom selectively. Adding a fluorine radical donor yields the benzylic
1-Cyano-1, 3-butadienes. II. Carbon Structure of the Adduct Formed by the Diels--Alder Condensation of 1-Cyano-1, 3-butadiene with 1, 3-Butadiene.
Snyder HR and Poos GI.
Journal of the American Chemical Society, 71(3), 1057-1058 (1949)
Yaws CL.
The Yaws Handbook of Vapor Pressure: Antoine coefficients , 234-234 (2015)

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持