C94807
3-吡啶甲腈
98%
别名:
3-氰基吡啶, 尼古丁腈, 烟酸腈
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关于此项目
经验公式（希尔记法）:
C6H4N2
化学文摘社编号:
分子量:
104.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-863-0
Beilstein/REAXYS Number:
107711
MDL number:
产品名称
3-吡啶甲腈, 98%
InChI key
GZPHSAQLYPIAIN-UHFFFAOYSA-N
InChI
1S/C6H4N2/c7-4-6-2-1-3-8-5-6/h1-3,5H
SMILES string
N#Cc1cccnc1
assay
98%
form
crystals
impurities
<2.5% acetone
bp
201 °C (lit.)
mp
48-52 °C (lit.)
Quality Level
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
190.4 °F
flash_point_c
88 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
Win-Long Chia et al.
International journal of molecular sciences, 14(9), 18809-18823 (2013-09-17)
A new series of teraryl 2-(4'-alkoxybiphen-4-yl)-5-cyanopyridines (nO-PPPyCN, n = 2-8) compounds, bearing a cyanopyridine terminus, were synthesized using a short 2-step reaction with overall yields between 33% and 69%. Spectral analyses were in accord with the expected structures. Thermotropic behavior
A Tanaka et al.
Journal of chromatography, 466, 307-317 (1989-04-19)
The determination of nicotinamide as 3-cyanopyridine after dehydration by heptafluorobutyric anhydride (HFB) was performed by gas-liquid chromatography (GLC) with flame ionization detection (GLC-FID) and a column of 5% OV-17 on Chromosorb W AW DMCS at 130 degrees C. Determination was
H Adolfsson et al.
The Journal of organic chemistry, 65(25), 8651-8658 (2000-12-12)
The epoxidation of alkenes with 30% aqueous hydrogen peroxide is catalyzed efficiently by methyltrioxorhenium (MTO) in the presence of pyridine additives. The addition of 1-10 mol % of 3-cyanopyridine increases the system's efficiency for terminal and trans-disubstituted alkenes resulting in
Anirban Banerjee et al.
Biotechnology and applied biochemistry, 37(Pt 3), 289-293 (2003-01-29)
A rapid, simple and sensitive fluorometric assay method for the determination of nitrilase activity is described. 3-Cyanopyridine was hydrolysed to nicotinic acid by Rhodococcus rhodochrous and the liberated NH(3) was allowed to react with buffered o -phthaldialdehyde-2-mercaptoethanol solution (pH 7.4)
Synthesis and antihistaminic activity of 2-guanadino-3-cyanopyridines and pyrido[2,3-d]-pyrimidines.
J M Quintela et al.
Bioorganic & medicinal chemistry, 5(8), 1543-1553 (1997-08-01)
2-Guanadino-3-cyanopyridines 8-33 and pyrido[2,3-d]-pyrimidines 35-52 were synthesized by nucleophilic displacement and cyclization of the chloroamidines 6a-d easily obtained by reaction of 2-aminocyanopyridines 5a-d with phosgene iminium chloride and their action on the release of histamine by mast cells examined under
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