CAS 1451393-34-2
:B-(3,4-Difluoro-5-formylphenyl)boronic acid
Description:
B-(3,4-Difluoro-5-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with difluoro and formyl groups. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The difluoro substitutions enhance its electronic properties, potentially influencing reactivity and solubility. The formyl group introduces a reactive aldehyde functionality, which can participate in further chemical transformations. In terms of physical properties, boronic acids generally have moderate solubility in polar solvents, and their stability can be affected by environmental conditions such as pH and temperature. This compound may also exhibit interesting optical properties due to the presence of fluorine atoms, which can affect its electronic structure. Overall, B-(3,4-Difluoro-5-formylphenyl)boronic acid is a versatile building block in the synthesis of complex organic molecules.
Formula:C7H5BF2O3
InChI:InChI=1S/C7H5BF2O3/c9-6-2-5(8(12)13)1-4(3-11)7(6)10/h1-3,12-13H
InChI key:InChIKey=UZXWYGACIABDHY-UHFFFAOYSA-N
SMILES:C(=O)C1=CC(B(O)O)=CC(F)=C1F
Synonyms:- Boronic acid, B-(3,4-difluoro-5-formylphenyl)-
- B-(3,4-Difluoro-5-formylphenyl)boronic acid
- (3,4-Difluoro-5-formylphenyl)boronic acid
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