推荐产品
品質等級
產品線
ReagentPlus®
化驗
99%
形狀
liquid
expl. lim.
0.34-6.3 %
折射率
n20/D 1.528 (lit.)
bp
191 °C (lit.)
mp
−13 °C (lit.)
SMILES 字串
N#Cc1ccccc1
InChI
1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H
InChI 密鑰
JFDZBHWFFUWGJE-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般說明
Benzonitrile, also known as a phenyl cyanide compound, is a useful solvent and a versatile precursor to many derivatives. It is a good solvent for the study of inorganic, organic, anhydrous, and organometallic compounds.
應用
Benzonitrile can be used as:
- An electrochemical solvent to investigate the electrochemistry, spectroscopic properties, and reactivity of a series of cobalt porphyrins with various substituents.
- Building block or starting material in various organic synthesis reactions.
- Employed in coupling reactions, such as Suzuki couplings or Heck reactions, to facilitate the formation of carbon-carbon bonds.
法律資訊
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Dermal - Acute Tox. 4 Oral
儲存類別代碼
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類（WGK）
WGK 1
閃點（°F）
158.0 °F - closed cup
閃點（°C）
70 °C - closed cup
其他客户在看
Purification of solvents for electroanalysis: benzonitrile; dichloromethane; 1, 1-dichloroethane and 1, 2-dichloroethane
Kadish KM, et al.
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 59(5), 703-714 (1987)
Vibrational fundamentals and natural bond orbitals analysis of some tri-fluorinated benzonitriles in ground state
Mukherjee V, et al.
Spectrochimica Acta Part A: Molecular Spectroscopy, 81(1), 609-619 (2011)
Electrochemistry and Spectroelectrochemistry of Cobalt Porphyrins with ?-Extending and/or Highly Electron-Withdrawing Pyrrole Substituents. In Situ Electrogeneration of ?-Bonded Complexes
Ke X, et al.
Inorganic Chemistry, 57(3), 1490-1503 (2018)
Yoshimitsu Hashimoto et al.
Organic & biomolecular chemistry, 10(30), 6003-6009 (2012-05-19)
A variety of highly functionalized polycyclic isoxazoles are prepared by a two-step protocol: (1) 1,3-dipolar cycloaddition of o,o'-disubstituted benzonitrile oxides to para-quinone mono-acetals, then (2) dehydrogenation. The cycloaddition proceeds in a regioselective manner, favouring the formation of the 4-acyl cycloadducts
A general and efficient heterogeneous gold-catalyzed hydration of nitriles in neat water under mild atmospheric conditions.
Yong-Mei Liu et al.
ChemSusChem, 5(8), 1392-1396 (2012-06-08)
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