Weight | 105.1 g/mol |
---|---|
Formula | C5H3N3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
Pyrazinecarbonitrile (19847-12-2)
cyanopyrazine
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- Nitrile hydratase-catalyzed production of isonicotinamide, picolinamide and pyrazinamide from 4-cyanopyridine, 2-cyanopyridine and cyanopyrazine in Rhodococcus rhodochrous J1 (Journal of Biotechnology, 1988)
- Bioconversion of 2-cyanopyrazine to 5-hydroxypyrazine-2-carboxylic acid with Agrobacterium sp. DSM 6336 (Applied Microbiology and Biotechnology, 1997)
- Synthesis and antimycobacterial properties of N-substituted 6-amino-5-cyanopyrazine-2-carboxamides (Bioorganic & Medicinal Chemistry, 2011)
- Synthesis and 1H and 13C NMR spectra of sulfur derivatives of pyrazine derived from amidation product of 2-chloropyrazine and 6-chloro-2-pyrazinecarbonitrile. Tuberculostatic activity (Collection of Czechoslovak Chemical Communications, 1990)
- Surface-enhanced Raman spectra of pyrazinecarboxamide and pyrazinecarbonitrile on silver sols (Journal of Raman Spectroscopy, 1992)
- Nitrilase-catalyzed production of pyrazinoic acid, an antimycobacterial agent, from cyanopyrazine by resting cells of Rhodococcus rhodochrous J1 (The Journal of Antibiotics, 1990)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cyanopyrazine
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SMILESC1=CN=C(C=N1)C#N
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InChIKeyPMSVVUSIPKHUMT-UHFFFAOYSA-N
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Similar Compounds
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2-(Chloromethyl)-3-methylpyrazine hydrochloride
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2-Hydroxy-3-methylpyrazine
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2-(Pyrazin-2-yl)ethanamine
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2-(pyrazin-2-yl)ethanol
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3-Methylpyrazine-2-carbaldehyde
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2-Bromo-3-methylpyrazine
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pyrazine-2-carbonyl chloride hydrochloride
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(3-chloropyrazin-2-yl)methanamine
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4-bromopyridine-2-carbonitrile
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2-Acetyl-3-ethylpyrazine
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methyl pyrazine-2-carboxylate
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55316-33-1
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Quinoxaline-2-carbaldehyde
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4-chloropyridine-2-carbonitrile
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quinoxalin-2-ylmethanol
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1H-Imidazole-2-carbonitrile
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