349496
2-氰基吡嗪
99%
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关于此项目
经验公式（希尔记法）:
C5H3N3
化学文摘社编号:
分子量:
105.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
243-369-5
MDL number:
Assay:
99%
Form:
liquid
产品名称
2-氰基吡嗪, 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
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
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
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
Reductive decyanation of pyrazinecarbonitriles.
Albaneze-Walker J, et al.
Tetrahedron Letters, 43(38), 6747-6750 (2002)
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
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
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