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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)-

5-Hydroxy-3-phenylbenzoic acid

Oc1cc(cc(c1)C(=O)O)c1ccccc1 Request for Quotation
Chemical Name: 5-Hydroxy-3-phenylbenzoic acid
CAS Number: 35489-88-4
Product Number: AG007AW0(AGN-PC-0WABGO)
Synonyms:
MDL No:
Molecular Formula: C13H10O3
Molecular Weight: 214.2167

Identification/Properties

Computed Properties
Molecular Weight:
214.22g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
214.062994g/mol
Monoisotopic Mass:
214.062994g/mol
Topological Polar Surface Area:
57.5Ų
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
246
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


5-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid is a versatile compound commonly utilized in chemical synthesis for its valuable applications in the field of organic chemistry. This acid derivative serves as a crucial building block in the creation of various pharmaceuticals and agrochemicals. Its unique chemical structure enables it to participate in diverse reactions, leading to the synthesis of biologically active compounds. Additionally, 5-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid plays a significant role in the development of novel materials and specialty chemicals, showcasing its importance in the realm of synthetic organic chemistry.