CAS 1451392-98-5
:B-(2,6-Dichloro-4-formylphenyl)boronic acid
Description:
B-(2,6-Dichloro-4-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 two chlorine atoms and an aldehyde group. 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 dichloro substitution on the phenyl ring can influence its reactivity and solubility, while the formyl group may participate in further chemical transformations. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The specific structural features of B-(2,6-Dichloro-4-formylphenyl)boronic acid may also impart unique electronic properties, affecting its behavior in chemical reactions and interactions with biological systems. Overall, this compound represents a valuable building block in the development of complex organic molecules.
Formula:C7H5BCl2O3
InChI:InChI=1S/C7H5BCl2O3/c9-5-1-4(3-11)2-6(10)7(5)8(12)13/h1-3,12-13H
InChI key:InChIKey=JIIZYKDHZYFDOO-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=C(C=O)C=C1Cl
Synonyms:- B-(2,6-Dichloro-4-formylphenyl)boronic acid
- Boronic acid, B-(2,6-dichloro-4-formylphenyl)-
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