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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-(4-fluorophenyl)-

Fc1ccc(cc1)c1cc[nH]n1 Request for Quotation
Chemical Name: 1H-Pyrazole, 3-(4-fluorophenyl)-
CAS Number: 154258-82-9
Product Number: AG003I4G(AGN-PC-0O4E6S)
Synonyms:
MDL No:
Molecular Formula: C9H7FN2
Molecular Weight: 162.1637

Identification/Properties

Properties
MP:
100-102 °C
BP:
334.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
162.167g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
162.059g/mol
Monoisotopic Mass:
162.059g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
144
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(4-Fluorophenyl)pyrazole is a versatile building block in chemical synthesis due to its unique structural properties and reactivity. This compound is commonly used as a key intermediate in the development of various pharmaceuticals, agrochemicals, and materials science applications. Its molecular structure contains a pyrazole ring with a fluorophenyl group attached at the 3-position, providing opportunities for selective functionalization and derivatization.In chemical synthesis, 3-(4-Fluorophenyl)pyrazole serves as a valuable starting material for the construction of biologically active molecules such as potential anti-inflammatory agents, anti-cancer drugs, or enzyme inhibitors. Its distinct chemical reactivity allows for the formation of diverse chemical bonds through substitution, addition, or coupling reactions. Researchers and chemists utilize this compound to introduce specific functional groups or stereochemistry into target molecules, enabling precise control over the final product's properties and activities.Moreover, the presence of the fluorophenyl moiety in 3-(4-Fluorophenyl)pyrazole imparts unique physicochemical characteristics to the synthesized compounds, such as altered solubility, lipophilicity, or binding affinity. This feature enhances the pharmacokinetic profiles and biological activities of the derived products, making them potential candidates for further drug discovery or material design studies.Overall, the strategic utilization of 3-(4-Fluorophenyl)pyrazole in chemical synthesis offers a powerful tool for molecular design and innovation in various scientific fields, highlighting its significance as a valuable building block in the creation of novel compounds with diverse applications.