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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)-

4-(4-carboxyphenyl)-3-methylbenzoic acid

OC(=O)c1ccc(cc1)c1ccc(cc1C)C(=O)O Request for Quotation
Chemical Name: 4-(4-carboxyphenyl)-3-methylbenzoic acid
CAS Number: 1186048-28-1
Product Number: AG0075TK(AGN-PC-038WYS)
Synonyms:
MDL No:
Molecular Formula: C15H12O4
Molecular Weight: 256.2534

Identification/Properties

Computed Properties
Molecular Weight:
256.257g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
256.074g/mol
Monoisotopic Mass:
256.074g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
344
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


2-Methyl-[1,1'-biphenyl]-4,4'-dicarboxylic acid is a versatile compound commonly used in chemical synthesis for its unique properties. This acid is frequently employed as a building block in the creation of various organic molecules due to its ability to introduce specific functional groups and structural motifs. In particular, the 2-Methyl-[1,1'-biphenyl]-4,4'-dicarboxylic acid serves as a valuable intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and novel materials. Its molecular structure offers diverse reactivity, enabling chemists to tailor its use for a wide range of applications in the field of organic chemistry.