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Merck
CN

349496

Pyrazinecarbonitrile

99%

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About This Item

Empirical Formula (Hill Notation):
C5H3N3
CAS Number:
19847-12-2
Molecular Weight:
105.10
NACRES:
NA.22
PubChem Substance ID:
24861682
UNSPSC Code:
12352100
EC Number:
243-369-5
MDL number:
MFCD00049361

Key Documents

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Product Name

Pyrazinecarbonitrile, 99%

InChI key

PMSVVUSIPKHUMT-UHFFFAOYSA-N

InChI

1S/C5H3N3/c6-3-5-4-7-1-2-8-5/h1-2,4H

SMILES string

N#Cc1cnccn1

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

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

206.6 °F - closed cup

flash_point_c

97 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ5322
MKCX6234
MKCX2737
MKCV5653
0000229694

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Reductive decyanation of pyrazinecarbonitriles.
Albaneze-Walker J, et al.
Tetrahedron Letters, 43(38), 6747-6750 (2002)
Surface-enhanced Raman spectra of pyrazinecarboxamide and pyrazinecarbonitrile on silver sols.
Arenas JF, et al.
Journal of Raman Spectroscopy, 23(5), 249-252 (1992)
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
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
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