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Merck
모든 사진(1)

주요 문서

349496

Sigma-Aldrich

Pyrazinecarbonitrile

99%

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About This Item

실험식(Hill 표기법):
C5H3N3
CAS Number:
Molecular Weight:
105.10
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

99%

양식

liquid

refractive index

n20/D 1.534 (lit.)

bp

87 °C/6 mmHg (lit.)

density

1.174 g/mL at 25 °C (lit.)

작용기

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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픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

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

개인 보호 장비

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


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시험 성적서(COA)

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문서 라이브러리 방문

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
Surface-enhanced Raman spectra of pyrazinecarboxamide and pyrazinecarbonitrile on silver sols.
Arenas JF, et al.
Journal of Raman Spectroscopy, 23(5), 249-252 (1992)
Synthesis, structure, network and thermal analysis of four 5-(pyrazinyl) tetrazolato copper (II) and cobalt (II) complexes.
Abu-Youssef MAM, et al.
Polyhedron, 26(7), 1531-1540 (2007)
M Kobayashi et al.
The Journal of antibiotics, 43(10), 1316-1320 (1990-10-01)
Using resting cells of Rhodococcus rhodochrous J1, in which a large amount of nitrilase is induced, a simple and efficient bioconversion process for the production of pyrazinoic acid, an antimycobacterial agent, through catalysis by a nitrilase was developed. The reaction
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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