| Weight | 220.275 g/mol |
|---|---|
| Formula | C15H12N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 2 |
4,5-Diphenylimidazole (668-94-0)
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- Bis(acetato)bis(1-methyl-4,5-diphenylimidazole)copper(II): Preparation, characterization, crystal structure, DNA strand breakage and cytogenetic effect (Journal of Inorganic Biochemistry, 1998)
- 2-(4-Hydrazinocarbonylphenyl)-4,5-diphenylimidazole as a versatile fluorescent derivatization reagent for the high-performance liquid chromatographic analysis of free fatty acids (Journal of Chromatography B: Biomedical Sciences and Applications, 1993)
- A hierarchical self-assembly of 4,5-diphenylimidazole on copper (Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2006)
- Syntheses of azo dyes containing 4,5-diphenylimidazole and their evaluation as analytical reagents (Analytica Chimica Acta, 1976)
- Evidence for a hydrogen bonded dimer as a fluorescence quenching channel in 4,5-diphenylimidazole (Journal of Luminescence, 1991)
- Novel Regioselective Hydroxyl-Alkylation of 4,5-Diphenylimidazole-2-thione and a Competitive Intramolecular Ring Closure of the S-Hydroxyalkyl-imidazoles to Imidazo[2,1-b]thiazines and Thiazoles. Role of Catalyst, Microwave Irradiation, and Solid Support. (Nucleosides, Nucleotides & Nucleic Acids, 2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C2=C(N=CN2)C3=CC=CC=C3
-
InChIKeyCPHGOBGXZQKCKI-UHFFFAOYSA-N
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Synthesis
Reactant
+
CHLOROBENZENE
(Decarboxylative coupling)
Reactant
+
CHLOROBENZENE
(Stille)
Phenylboronic acid
+
Reactant
(Suzuki)
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3-(6-iodoimidazo[1,2-a]pyridin-2-yl)aniline
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2-phenylimidazo[1,2-a]pyrimidine-3-carbaldehyde
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2-(4-Fluorophenyl)pyridine
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4,5-diphenyl-1,3-thiazol-2-amine
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4-Chloro-2,6-diphenylpyrimidine
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4,5-Diphenylimidazole
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