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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)-

[1,1'-Biphenyl]-2-carboxylicacid, 2'-(hydroxymethyl)-

OCc1ccccc1c1ccccc1C(=O)O Request for Quotation
Chemical Name: [1,1'-Biphenyl]-2-carboxylicacid, 2'-(hydroxymethyl)-
CAS Number: 18773-63-2
Product Number: AG002GGW(AGN-PC-0JKKLG)
Synonyms:
MDL No:
Molecular Formula: C14H12O3
Molecular Weight: 228.2433

Identification/Properties

Properties
BP:
432.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
228.247g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
228.079g/mol
Monoisotopic Mass:
228.079g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
264
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


2'-(Hydroxymethyl)-[1,1'-biphenyl]-2-carboxylic acid is a versatile compound used in chemical synthesis for the production of various pharmaceuticals, agrochemicals, and materials. It serves as a key building block in the synthesis of complex organic molecules due to its unique structure and reactivity. With its functional groups, this compound can participate in a wide range of reactions, including esterification, amidation, and cross-coupling reactions, to afford structurally diverse products. This compound is particularly valuable in the development of new drugs and materials with potential applications in the fields of medicine, agriculture, and materials science.