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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]-3,3'-dicarboxylic acid

OC(=O)c1cccc(c1)c1cccc(c1)C(=O)O Request for Quotation
Chemical Name: [1,1'-Biphenyl]-3,3'-dicarboxylic acid
CAS Number: 612-87-3
Product Number: AG00EJ85(AGN-PC-0JM1YO)
Synonyms:
MDL No:
Molecular Formula: C14H10O4
Molecular Weight: 242.2268

Identification/Properties

Properties
MP:
>300°C (dec.)
BP:
524.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
242.23g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
242.058g/mol
Monoisotopic Mass:
242.058g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
294
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Biphenyl-3,3'-dicarboxylic acid is a versatile compound commonly used in chemical synthesis for its unique applications. Its rigid and planar structure makes it a valuable building block in the preparation of various organic molecules. In chemical synthesis, Biphenyl-3,3'-dicarboxylic acid is often employed as a key intermediate in the synthesis of complex organic compounds, particularly in the pharmaceutical and materials science industries. Its ability to undergo various chemical reactions, such as esterification, amidation, and Grignard reactions, allows for the introduction of functional groups at specific positions on the biphenyl core.One notable application of Biphenyl-3,3'-dicarboxylic acid is in the synthesis of liquid crystal materials. By introducing specific substituents to the biphenyl core, researchers can tailor the properties of the resulting liquid crystal, such as its optical characteristics, melting point, and stability. This enables the design of liquid crystal materials with desired properties for applications ranging from displays to advanced materials.Overall, the use of Biphenyl-3,3'-dicarboxylic acid in chemical synthesis showcases its importance as a versatile and valuable building block in the creation of diverse organic molecules with tailored properties and applications.