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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
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
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
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)
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
Li-Qun Jin et al.
New biotechnology, 28(6), 610-615 (2011-05-10)
2-Chloronicotinic acid is receiving much attention for its effective applications as a key precursor in the synthesis of pesticides and medicines. In this study, a strain ZJB-09149 converting 2-chloro-3-cyanopyridine to 2-chloronicotinic acid was newly isolated and identified as Rhodococcus erythropolis
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