| Weight | 180.21 g/mol |
|---|---|
| Formula | C12H8N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
PHENAZINE (92-82-0)
Score:
#1937 in Physics
,
#4759 in Biology
,
#6062 in Chemistry
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- The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen (Biochemical and Biophysical Research Communications, 1972)
- Role of a phenazine antibiotic from Pseudomonas fluorescens in biological control of Gaeumannomyces graminis var. tritici. (Journal of Bacteriology, 1988)
- Microbial phenazine production enhances electron transfer in biofuel cells (Environmental Science & Technology, 2005)
- Functional Analysis of Genes for Biosynthesis of Pyocyanin and Phenazine-1-Carboxamide from Pseudomonas aeruginosa PAO1 (Journal of Bacteriology, 2001)
- Production of the antibiotic phenazine-1-carboxylic Acid by fluorescent pseudomonas species in the rhizosphere of wheat. (Applied and Environmental Microbiology, 1990)
- Synthesis and Properties of Diamino-Substituted Dipyrido (3,2-a:2',3'-c)phenazine. (Bulletin of the Chemical Society of Japan, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)N=C3C=CC=CC3=N2
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InChIKeyPCNDJXKNXGMECE-UHFFFAOYSA-N
- Pubchem - PHENAZINE
- Wikipedia - dibenzopyrazine
Phenazine is an organic compound with the formula (C6H4)2N2. It is a dibenzo annulated pyrazine, and the parent substance of many dyestuffs, such as the toluylene red, indulines, and safranines (and the closely related eurhodines). Phenazine crystallizes in yellow needles, which are only sparingly soluble in alcohol.
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6-AZAINDOLE
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quinoxaline-2-carbonitrile
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PHENAZINE
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