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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-carboxylic acid, 4'-(bromomethyl)-, methyl ester

COC(=O)c1ccccc1c1ccc(cc1)CBr Request for Quotation
Chemical Name: [1,1'-Biphenyl]-2-carboxylic acid, 4'-(bromomethyl)-, methyl ester
CAS Number: 114772-38-2
Product Number: AG000F70(AGN-PC-0NEEYL)
Synonyms:
MDL No:
Molecular Formula: C15H13BrO2
Molecular Weight: 305.1665

Identification/Properties

Properties
MP:
56 °C
BP:
412.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
305.171g/mol
XLogP3:
4.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
304.01g/mol
Monoisotopic Mass:
304.01g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
272
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 4'-(bromomethyl)-[1,1'-biphenyl]-2-carboxylate is a versatile compound commonly employed in chemical synthesis as a building block for the preparation of various organic molecules. By utilizing the bromomethyl functionality on the biphenyl core, this compound offers strategic opportunities for the introduction of diverse chemical motifs through substitution reactions. This enables chemists to efficiently access structurally complex molecules with tailored properties for applications in pharmaceuticals, materials science, and agrochemicals. Furthermore, the carboxylate ester group in the molecule can serve as a convenient handle for further functionalization, allowing for the facile modification of its chemical properties. In the realm of organic synthesis, Methyl 4'-(bromomethyl)-[1,1'-biphenyl]-2-carboxylate proves to be a valuable tool for the construction of intricate molecular architectures with precise control over stereochemistry and functionality, thereby facilitating the development of innovative compounds with potential implications across various scientific disciplines.