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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)-

Benzoic acid, 4-methyl-3-(trifluoromethyl)-

OC(=O)c1ccc(c(c1)C(F)(F)F)C Request for Quotation
Chemical Name: Benzoic acid, 4-methyl-3-(trifluoromethyl)-
CAS Number: 261952-01-6
Product Number: AG002S7G(AGN-PC-0KKWYN)
Synonyms:
MDL No:
Molecular Formula: C9H7F3O2
Molecular Weight: 204.1459

Identification/Properties

Computed Properties
Molecular Weight:
204.148g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
204.04g/mol
Monoisotopic Mass:
204.04g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
225
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methyl-3-(trifluoromethyl)benzoic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties. In organic chemistry, this compound serves as a crucial building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the molecules it is incorporated into, making it particularly useful in drug discovery and development. Furthermore, the presence of the methyl group allows for tailored modifications to fine-tune the compound's reactivity and selectivity in chemical reactions.In the field of material science, 4-Methyl-3-(trifluoromethyl)benzoic acid is utilized as a precursor in the synthesis of functional materials such as liquid crystals, polymers, and advanced coatings. Its unique structural features contribute to the design and development of novel materials with specific properties, such as high thermal stability and optical clarity.Overall, the application of 4-Methyl-3-(trifluoromethyl)benzoic acid in chemical synthesis enables researchers and chemists to access a wide range of functionalized compounds and materials with tailored properties for diverse industrial applications.