349496
Pyrazinecarbonitrile
99%
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About This Item
Empirical Formula (Hill Notation):
C5H3N3
CAS Number:
Molecular Weight:
105.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.534 (lit.)
bp
87 °C/6 mmHg (lit.)
density
1.174 g/mL at 25 °C (lit.)
functional group
nitrile
SMILES string
N#Cc1cnccn1
InChI
1S/C5H3N3/c6-3-5-4-7-1-2-8-5/h1-2,4H
InChI key
PMSVVUSIPKHUMT-UHFFFAOYSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
206.6 °F - closed cup
Flash Point(C)
97 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Derrick R Seiner et al.
Biochemistry, 49(44), 9613-9619 (2010-10-01)
Nicotinamidase/pyrazinamidase (PncA) is involved in the NAD+ salvage pathway of Mycobacterium tuberculosis and other bacteria. In addition to hydrolyzing nicotinamide into nicotinic acid, PncA also hydrolyzes the prodrug pyrazinamide to generate the active form of the drug, pyrazinoic acid, which
Il Woong Baek et al.
Journal of nanoscience and nanotechnology, 10(10), 6939-6943 (2010-12-09)
We have fabricated fluorescing polystyrene/dicyanopyrazine-linked porphyrin (PS/4-TDCPP) nanofibers using the electrospinning technique. UV-vis spectroscopy shows a strong Soret band and two relatively weak Q bands from the PS/4-TDCPP films and fibers, and reveals that the 4-TDCPP molecules are homogeneously dispersed
Reductive decyanation of pyrazinecarbonitriles.
Albaneze-Walker J, et al.
Tetrahedron Letters, 43(38), 6747-6750 (2002)
Katarzyna Gobis et al.
Acta poloniae pharmaceutica, 63(1), 39-45 (2007-05-23)
The new pyrazine derivatives exhibiting an antibacterial activity have been synthesized. Initial amidoxime 1 was obtained in the reaction of pyrazinecarbonitrile with hydroxylamine. Upon treatment of amidoxime with methyl iodide O-methyl derivative 2 was formed. Both amidoximes were transformed into
Jan Zitko et al.
Bioorganic & medicinal chemistry, 19(4), 1471-1476 (2011-01-29)
A series of fifteen new compounds related to pyrazinamide (PZA) were synthesized, characterized with analytical data and screened for antimycobacterial, antifungal and antibacterial activity. The series consists of 6-chloro-5-cyanopyrazine-2-carboxamide and N-substituted 6-amino-5-cyanopyrazine-2-carboxamides, derived from the previous by nucleophilic substitution with
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