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C94807

Sigma-Aldrich

3-Pyridinecarbonitrile

98%

Sinónimos:

3-Cyanopyridine, Nicotinic acid nitrile, Nicotinonitrile

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About This Item

Fórmula empírica (notación de Hill):
C6H4N2
Número de CAS:
100-54-9
Peso molecular:
104.11
Beilstein/REAXYS Number:
107711
EC Number:
202-863-0
MDL number:
MFCD00006372
UNSPSC Code:
12352100
PubChem Substance ID:
24893001
NACRES:
NA.22

Quality Level

100

assay

98%

form

crystals

impurities

<2.5% acetone

bp

201 °C (lit.)

mp

48-52 °C (lit.)

SMILES string

N#Cc1cccnc1

InChI

1S/C6H4N2/c7-4-6-2-1-3-8-5-6/h1-3,5H

InChI key

GZPHSAQLYPIAIN-UHFFFAOYSA-N

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Categorías relacionadas

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

190.4 °F

flash_point_c

88 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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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