| Weight | 220.275 g/mol |
|---|---|
| Formula | C15H12N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 2 |
3,5-Diphenylpyrazole (1145-01-3)
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- Novel 1,5-diphenylpyrazole nonnucleoside HIV-1 reverse transcriptase inhibitors with enhanced activity versus the delavirdine-resistant P236L mutant : Lead identification and SAR of 3- and 4-substituted derivatives (Journal of Medicinal Chemistry, 2000)
- Syntheses and x-ray structures of group 11 pyrazole and pyrazolate complexes. X-ray crystal structures of bis(3,5-diphenylpyrazole)copper(II) dibromide, tris(.mu.-3,5-diphenylpyrazolato-N,N')trisilver(I)-2-tetrahydrofuran, tris(.mu.-3,5-diphenylpyrazolato-N,N')trigold(I), and hexakis(.mu.-3,5-diphenylpyrazolato-N,N')hexagold(I) (Inorganic Chemistry, 1988)
- Synthesis, X-ray structure, and catalytic properties of the unprecedented tetranuclear copper(I) species [Cu(dppz)]4 (Hdppz = 3,5-diphenylpyrazole) (Inorganic Chemistry, 1994)
- A convenient and efficient protocol for the synthesis of 5-aryl-1,3-diphenylpyrazole catalyzed by hydrochloric acid under ultrasound irradiation (Ultrasonics Sonochemistry, 2010)
- The influence of the nitro group on the solid-state structure of 4-nitropyrazoles: the cases of pyrazole, 3,5-dimethylpyrazole, 3,5-di-tert-butylpyrazole and 3,5-diphenylpyrazole. I. Static aspects (crystallography and thermodynamics) (Acta Crystallographica Section B-structural Science, 1994)
- Reactions of lanthanoid metals with 3,5-diphenylpyrazole at elevated temperatures: synthesis and structures of both homoleptic, [Ln3(Ph2pz)9](Ln = La, Nd), [Ln2(Ph2pz)6](Ln = Er, Lu), and heteroleptic, [Ln(Ph2pz)3(Ph2pzH)2](Ln = La, Nd, Gd, Tb, Er or Yb), pyrazolate complexes (Dalton Transactions, 2004)
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CHLOROBENZENE
(Decarboxylative coupling)
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