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CAS 91853-46-2

:

[1,1'-Biphenyl]-4-propanoic acid, .alpha.-oxo-

Description:
[1,1'-Biphenyl]-4-propanoic acid, α-oxo- (CAS 91853-46-2) is an organic compound characterized by its biphenyl structure with a propanoic acid functional group and an α-oxo substituent. This compound typically exhibits properties associated with both aromatic and aliphatic systems, including moderate solubility in organic solvents and potential reactivity due to the presence of the carboxylic acid group. The α-oxo functionality suggests the presence of a carbonyl group adjacent to the propanoic acid moiety, which may influence its reactivity and interactions with other chemical species. This compound may be of interest in various fields, including pharmaceuticals and materials science, due to its potential as a building block in organic synthesis or as a precursor to more complex molecules. Its stability, melting point, boiling point, and specific reactivity would depend on the surrounding conditions and the presence of other functional groups in a given reaction environment. Safety data and handling precautions should be consulted when working with this substance.
Formula:C15H12O3
Synonyms:
  • [1,1'-Biphenyl]-4-propanoic acid, α-oxo
  • 3-([1,1'-Biphenyl]-4-yl)-2-oxopropanoic acid
  • [1,1'-Biphenyl]-4-propanoic acid, α-oxo-
  • 3-(4-Biphenylyl)-2-oxopropanoic Acid
  • [1,1'-Biphenyl]-4-propanoic acid, .alpha.-oxo-
  • 2-oxo-3-(4-phenylphenyl)propanoic acid
  • 1,1'-Biphenyl]-4-propanoic acid, α-oxo
  • 4-Biphenylylpyruvic Acid
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Found 2 products.
  • 4-Biphenylylpyruvic Acid
    TRC
    + Info

    4-Biphenylylpyruvic Acid

    Controlled Product
    CAS:
    Formula:C15H12O3
    Color and Shape:Neat
    Molecular weight:240.254

    Ref: TR-B397870

    5g
    1,509.00€
  • 2-Oxo-3-(4-phenylphenyl)propanoic acid
    Biosynth
    + Info

    2-Oxo-3-(4-phenylphenyl)propanoic acid

    CAS:
    <p>2-Oxo-3-(4-phenylphenyl)propanoic acid is a chiral molecule that can be synthesized from 4-bromocinnamic acid and 2,3-dichlorobenzoyl chloride in two steps. The first step is an acid dehydrogenation of the 4-bromocinnamic acid to form the corresponding enol form. The second step is an arylation using 2,3-dichlorobenzoyl chloride. This compound has been found to be highly efficient and selective in its chemoenzymatic synthesis. Promiscuity of this compound has also been observed, which allows it to be used for the synthesis of various other compounds.</p>
    Formula:C15H12O3
    Purity:Min. 95%
    Molecular weight:240.25 g/mol

    Ref: 3D-RDA85346

    1g
    1,013.00€
    100mg
    377.00€