270318
苯甲腈
suitable for HPLC, 99.9%
别名:
苯基腈
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关于此项目
线性分子式:
C6H5CN
化学文摘社编号:
分子量:
103.12
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39031505
UNSPSC Code:
12190000
EC Number:
202-855-7
MDL number:
Beilstein/REAXYS Number:
506893
Assay:
99.9%
Grade:
HPLC grade
Technique(s):
HPLC: suitable
Bp:
191 °C (lit.)
SMILES string
N#Cc1ccccc1
InChI key
JFDZBHWFFUWGJE-UHFFFAOYSA-N
InChI
1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H
grade
HPLC grade
assay
99.9%
form
liquid
purified by
glass distillation
expl. lim.
0.34-6.3 %
technique(s)
HPLC: suitable
impurities
≤0.03% water
evapn. residue
<0.0005%
bp
191 °C (lit.)
mp
−13 °C (lit.)
λ
H2O reference
UV absorption
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
application(s)
food and beverages
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
flash_point_f
158.0 °F - closed cup
flash_point_c
70 °C - closed cup
法规信息
危险化学品
此项目有
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)
Benzonitrile and acetonitrile complexes of ruthenium ammines.
Clarke RE and Ford PC.
Inorganic Chemistry, 9(2), 227-235 (1970)
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
Microwave spectra of isotopic benzonitriles. Refined molecular structure of benzonitrile.
Casado J, et al.
Journal of Molecular Structure, 8(1-2), 211-224 (1971)
Johanna Ungersboeck et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 70(11), 2615-2620 (2012-09-04)
The intention for the present study was to implement a microfluidic set-up for N-(11)C-methylations in a flow-through microreactor device with [(11)C]DASB as model-compound and [(11)C]CH(3)I and [(11)C]CH(3)OTf, respectively, as (11)C-methylation agents. Due to an observed "aging" effect of the (11)C-methylation
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