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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-carboxylicacid, 4'-formyl-

O=Cc1ccc(cc1)c1cccc(c1)C(=O)O Request for Quotation
Chemical Name: [1,1'-Biphenyl]-3-carboxylicacid, 4'-formyl-
CAS Number: 222180-20-3
Product Number: AG003LGJ(AGN-PC-0KL72A)
Synonyms:
MDL No:
Molecular Formula: C14H10O3
Molecular Weight: 226.2274

Identification/Properties

Properties
MP:
188-192°C(lit.)
BP:
456.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
226.231g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
226.063g/mol
Monoisotopic Mass:
226.063g/mol
Topological Polar Surface Area:
54.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
279
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:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4'-Formyl-[1,1'-biphenyl]-3-carboxylic acid, a versatile chemical compound, finds widespread applications in chemical synthesis. Its aldehyde functional group offers a key point of reactivity, enabling it to participate in various synthetic pathways. This compound serves as a crucial building block in the preparation of diverse organic molecules, owing to its ability to undergo various types of reactions such as condensation, nucleophilic addition, and oxidation. In organic synthesis, it can be utilized for the construction of complex molecules by forming carbon-carbon and carbon-heteroatom bonds. Furthermore, the presence of the biphenyl backbone in this compound imparts unique structural features to the synthesized compounds, making it highly valuable for medicinal chemistry, materials science, and other fields requiring tailored molecular architectures.