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About This Item
Empirical Formula (Hill Notation):
C6H4N2
CAS Number:
Molecular Weight:
104.11
Beilstein:
107711
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
190.4 °F
Flash Point(C)
88 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Zhongyi Cheng et al.
Molecules (Basel, Switzerland), 25(20) (2020-10-23)
High thermostability and catalytic activity are key properties for nitrile hydratase (NHase, EC 4.2.1.84) as a well-industrialized catalyst. In this study, rational design was applied to tailor the thermostability of NHase from Pseudonocardia thermophila JCM3095 (PtNHase) by combining FireProt server
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
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
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
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