CAS 915201-06-8
:Boronic acid, (4-chloro-3-hydroxyphenyl)-
Description:
Boronic acid, (4-chloro-3-hydroxyphenyl)-, with the CAS number 915201-06-8, is an organic compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenolic structure. This compound features a chloro substituent at the para position and a hydroxy group at the meta position relative to the boronic acid group on the aromatic ring. The presence of the boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The hydroxy group contributes to its solubility in polar solvents and can participate in hydrogen bonding, while the chloro group can serve as a leaving group in nucleophilic substitution reactions. Overall, this compound exhibits properties typical of boronic acids, including reactivity towards diols and potential applications in drug development and materials science. Its specific characteristics, such as melting point, boiling point, and solubility, would require further empirical data for precise determination.
Formula:C6H6BClO3
Synonyms:- 4-Chloro-3-Hydroxyphenylboronic Acid
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Found 3 products.
(4-Chloro-3-hydroxyphenyl)boronic acid
CAS:Formula:C6H6BClO3Purity:95%Color and Shape:SolidMolecular weight:172.37404-Chloro-3-hydroxybenzeneboronic acid
CAS:4-Chloro-3-hydroxybenzeneboronic acidPurity:98%Color and Shape:SolidMolecular weight:172.37g/mol(4-Chloro-3-hydroxyphenyl)boronic acid
CAS:Formula:C6H6BClO3Purity:97%Color and Shape:SolidMolecular weight:172.37


