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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)-

3-(3-methylphenyl)-5-nitrobenzoic acid

Cc1cccc(c1)c1cc(cc(c1)C(=O)O)[N+](=O)[O-] Request for Quotation
Chemical Name: 3-(3-methylphenyl)-5-nitrobenzoic acid
CAS Number: 1261953-03-0
Product Number: AG000S8X(AGN-PC-09Q4KM)
Synonyms:
MDL No:
Molecular Formula: C14H11NO4
Molecular Weight: 257.2414

Identification/Properties

Computed Properties
Molecular Weight:
257.245g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
257.069g/mol
Monoisotopic Mass:
257.069g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
352
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


3'-Methyl-5-nitro-[1,1'-biphenyl]-3-carboxylic acid, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis. This compound is valued for its ability to serve as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, $name$ plays a crucial role as a precursor in the formation of complex organic molecules through processes such as nitration, reduction, and condensation reactions. By incorporating $name$ into synthetic pathways, chemists can efficiently access a diverse array of functionalized biphenyl derivatives, offering new opportunities for drug discovery and material science research. Additionally, the unique structural features of $name$ contribute to its significance as a valuable intermediate in the development of novel and biologically active compounds with potential applications in medicine and industry.