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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Pyrazole, 3,5-diphenyl-

c1ccc(cc1)c1[nH]nc(c1)c1ccccc1 Request for Quotation
Chemical Name: 1H-Pyrazole, 3,5-diphenyl-
CAS Number: 1145-01-3
Product Number: AG000EL7(AGN-PC-03FKHV)
Synonyms:
MDL No:
Molecular Formula: C15H12N2
Molecular Weight: 220.2692

Identification/Properties

Computed Properties
Molecular Weight:
220.275g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
220.1g/mol
Monoisotopic Mass:
220.1g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
229
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Diphenyl-1H-pyrazole is a versatile compound widely used in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and materials. Due to its unique structural properties, this compound plays a crucial role in the development of organic compounds with diverse functionalities. In organic synthesis, 3,5-Diphenyl-1H-pyrazole serves as a valuable building block for the preparation of pyrazole derivatives, which exhibit a broad spectrum of biological activities such as antimicrobial, anticancer, and anti-inflammatory properties. Additionally, its reactivity and stability make it an essential component in the creation of advanced materials with tailored properties for applications in the fields of electronics, catalysis, and pharmaceutical formulations. By incorporating 3,5-Diphenyl-1H-pyrazole into synthetic pathways, chemists can access a wide range of structurally diverse compounds with significant potential for industrial and scientific advancements.