推荐产品
化驗
99.9%
形狀
liquid
純化經由
glass distillation
expl. lim.
0.34-6.3 %
技術
HPLC: suitable
雜質
≤0.03% water
蒸發殘留物
<0.0005%
折射率
n20/D 1.528 (lit.)
bp
191 °C (lit.)
mp
−13 °C (lit.)
&lambda ；
H2O reference
紫外吸收
λ: 300 nm Amax: 1.0
λ: 310 nm Amax: 0.40
λ: 335 nm Amax: 0.03
λ: 360-400 nm Amax: 0.01
應用
food and beverages
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
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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
Microwave spectra of isotopic benzonitriles. Refined molecular structure of benzonitrile.
Casado J, et al.
Journal of Molecular Structure, 8(1-2), 211-224 (1971)
Kenji Ueura et al.
Organic letters, 7(11), 2229-2231 (2005-05-20)
[reaction: see text]. The Suzuki-Miyaura-type cross-coupling of arylboron compounds with aryl halides proceeds efficiently in the presence of a rhodium-based catalyst system to produce the corresponding biaryls. Furthermore, it has unexpectedly been observed that the treatment with benzonitrile under similar
Benzonitrile and acetonitrile complexes of ruthenium ammines.
Clarke RE and Ford PC.
Inorganic Chemistry, 9(2), 227-235 (1970)
Lanthanide-imido complexes and their reactions with benzonitrile.
Dongmei Cui et al.
Angewandte Chemie (International ed. in English), 44(6), 959-962 (2004-12-22)
A multiphase reaction medium including pressurized carbon dioxide and water for selective hydrogenation of benzonitrile with a Pd/Al2O3 catalyst.
Yoshida H, et al.
Applied Catalysis A: General, 456, 215-222 (2013)
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