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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]-4-carboxylic acid, 4'-cyano-

N#Cc1ccc(cc1)c1ccc(cc1)C(=O)O Request for Quotation
Chemical Name: [1,1'-Biphenyl]-4-carboxylic acid, 4'-cyano-
CAS Number: 5728-46-1
Product Number: AG00EBEE(AGN-PC-0KKM5G)
Synonyms:
MDL No:
Molecular Formula: C14H9NO2
Molecular Weight: 223.2268

Identification/Properties

Properties
MP:
263-266 °C
BP:
443°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
223.231g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
223.063g/mol
Monoisotopic Mass:
223.063g/mol
Topological Polar Surface Area:
61.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
314
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile compound that finds application in various chemical synthesis processes. Specifically, 4'-Cyano-[1,1'-biphenyl]-4-carboxylic acid is utilized as a key building block in the creation of complex organic molecules. Its unique structure and reactivity make it ideal for diverse reactions, including cross-coupling, nucleophilic addition, and substitution reactions. By incorporating this compound into synthetic pathways, chemists can efficiently access a wide range of functionalized biphenyl derivatives and other valuable products with enhanced chemical properties.