所有图片(1)
About This Item
线性分子式:
C2H5C6H4CN
CAS号:
分子量:
131.17
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
方案
98%
折射率
n20/D 1.527 (lit.)
沸点
237 °C (lit.)
密度
0.956 g/mL at 25 °C (lit.)
官能团
nitrile
SMILES字符串
CCc1ccc(cc1)C#N
InChI
1S/C9H9N/c1-2-8-3-5-9(7-10)6-4-8/h3-6H,2H2,1H3
InChI key
SXFFMFAQNAFSLF-UHFFFAOYSA-N
一般描述
4-Ethylbenzonitrile is an electron deficient aromatic nitrile.
应用
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
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
208.0 °F - closed cup
闪点(°C)
97.8 °C - closed cup
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
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
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
Polystyrene Backbone Polymers Consisting of Alkyl-Substituted Triazine Side Groups for Phosphorescent OLEDs.
Salert BCD, et al.
Advances in Materials Science and Engineering (2012)
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)
Alkylphenols and arylnitriles in a biologically active neutral subfraction of cigarette smoke condensate.
Miller RL and Stedman RL.
Phytochemistry, 10(5), 1135-1140 (1971)
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.
联系技术服务部门