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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)-

2-fluoro-5-[4-(trifluoromethyl)phenyl]benzoic acid

OC(=O)c1cc(ccc1F)c1ccc(cc1)C(F)(F)F Request for Quotation
Chemical Name: 2-fluoro-5-[4-(trifluoromethyl)phenyl]benzoic acid
CAS Number: 1179671-81-8
Product Number: AG0081D3(AGN-PC-09PV07)
Synonyms:
MDL No:
Molecular Formula: C14H8F4O2
Molecular Weight: 284.2057

Identification/Properties

Computed Properties
Molecular Weight:
284.21g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
284.046g/mol
Monoisotopic Mass:
284.046g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
348
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Fluoro-4'-(trifluoromethyl)-[1,1'-biphenyl]-3-carboxylic acid is a versatile chemical compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as an important building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, 4-Fluoro-4'-(trifluoromethyl)-[1,1'-biphenyl]-3-carboxylic acid acts as a valuable intermediate for the preparation of more complex molecules. Its fluoro and trifluoromethyl substituents contribute to its ability to participate in diverse chemical reactions, such as cross-coupling reactions, nucleophilic substitutions, and transition metal-catalyzed transformations.This compound's presence in the structure of the target molecule can enhance its stability, lipophilicity, and biological activity. The fluorine atom provides unique properties that can influence the compound's pharmacokinetic profile, while the trifluoromethyl group can modulate the compound's physicochemical properties.Overall, the application of 4-Fluoro-4'-(trifluoromethyl)-[1,1'-biphenyl]-3-carboxylic acid in chemical synthesis enables the efficient construction of complex organic compounds with desired functionalities for a wide range of applications in the fields of pharmaceuticals, agrochemicals, and materials science.