| Weight | 144.177 g/mol |
|---|---|
| Formula | C9H8N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
1-Phenylimidazole (7164-98-9)
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- Enzyme kinetic and spectroscopic studies of inhibitor and effector interactions with indoleamine 2,3-dioxygenase. 1. Norharman and 4-phenylimidazole binding to the enzyme as inhibitors and heme ligands. (Biochemistry, 1989)
- The Metalation of 1-Methyl-, 1-Benzyl- and 1-Phenylimidazole with n-Butyllithium (Journal of the American Chemical Society, 1957)
- Synthesis and SAR study of new phenylimidazole-pyrazolo[1,5-c]quinazolines as potent phosphodiesterase 10A inhibitors. (Bioorganic & Medicinal Chemistry, 2011)
- Formation of organotin-nitrogen bonds IV. N-trialkyltin derivatives of 4-mono- or 4,5-disubstituted 1,2,3-triazoles, 3-phenyl-1,2,4-triazole, 3-phenylpyrazole and 4-phenylimidazole (Journal of Organometallic Chemistry, 1972)
- Selectivity of 1-phenylimidazole as a ligand for cytochrome P-450 and as an inhibitor of microsomal oxidation (Biochemical Pharmacology, 1983)
- Preparations and Characterization of Cyclopalladated Complexes of 1-Ethyl-2-phenylimidazole (Bulletin of the Chemical Society of Japan, 1979)
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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=C(C=C1)N2C=CN=C2
-
InChIKeySEULWJSKCVACTH-UHFFFAOYSA-N
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