| Weight | 264.284 g/mol |
|---|---|
| Formula | C16H12N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
1,5-diphenyl-1H-pyrazole-3-carboxylic acid (13599-22-9)
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- Functionalization and cyclization reactions of 4-benzoyl-1,5-diphenyl- 1H-pyrazole-3-carboxylic acid (Journal of Heterocyclic Chemistry, 1997)
- Further derivatives of 4-benzoyl-1,5-diphenyl-1H-pyrazole-3-carboxylic acid and their antibacterial activities (Medicinal Chemistry Research, 2007)
- 4Benzoyl1,5diphenyl1Hpyrazole3carboxylic acid methanol solvate (Acta Crystallographica Section E: Crystallographic Communications, 2005)
- Experimental and Theoretical Studies on the Functionalization Reactions of 4-Benzoyl-1,5-Diphenyl-1H-Pyrazole-3-Carboxylic Acid and Acid Chloride with 2,3-Diaminopyridine (Molecules, 2005)
- Synthesis and some reactions of 4-(ethoxycarbonyl)-1,5-diphenyl-1H-pyrazole-3-carboxylic acid (Journal of Heterocyclic Chemistry, 2007)
- Experimental and theoretical studies on the functionalization reactions of 4-benzoyl-1,5-diphenyl-1H-pyrazole-3-carboxylic acid and-acid chloride with various aminophenols (Structural Chemistry, 2006)
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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)C2=CC(=NN2C3=CC=CC=C3)C(=O)O
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InChIKeyJJMZLVASVSISLC-UHFFFAOYSA-N
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Synthesis
Phenylboronic acid
+
Reactant
(N-arylation heterocycles)
Reactant
+
CHLOROBENZENE
(Suzuki)
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