2538-50-3 Purity
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Specification
A copper-promoted coupling of phenylacetone and arylhydrazine was developed for the synthesis of 1,3-diarylpyrazoles from commercial substrates and/or simple transformations.
The reactions afforded substituted pyrazoles in the presence of TEMPO oxidant, acetic acid additive, and DMF solvent. A number of functionalities were compatible with reaction conditions, including halogens, methoxy, trifluoromethyl, and nitro groups. An indazole could be obtained if an electron-poor propiophenone was used.
The molecular formula of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is C15H14N2.
The molecular weight of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is 222.28 g/mol.
1,3-Diphenyl-4,5-dihydro-1H-pyrazole was created on March 26, 2005.
The IUPAC name of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is 2,5-diphenyl-3,4-dihydropyrazole.
The InChI of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is InChI=1S/C15H14N2/c1-3-7-13(8-4-1)15-11-12-17(16-15)14-9-5-2-6-10-14/h1-10H,11-12H2.
The InChIKey of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is ZWCZPVMIHLKVLD-UHFFFAOYSA-N.
The canonical SMILES of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is C1CN(N=C1C2=CC=CC=C2)C3=CC=CC=C3.
The CAS number of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is 2538-52-5.
The ChEMBL ID of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is CHEMBL1305810.
The topological polar surface area of 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is 15.6Ų.