CAS 736989-98-3
:Boronic acid,B-[3-(3-hydroxypropyl)phenyl]-
Description:
Boronic acid, B-[3-(3-hydroxypropyl)phenyl]- (CAS 736989-98-3), is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a hydroxypropyl group. This compound typically exhibits properties common to 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 hydroxypropyl substituent enhances its solubility in polar solvents and may influence its reactivity and interaction with biological systems. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, the presence of the hydroxyl group can impart unique properties, such as increased hydrogen bonding capabilities, which may affect the compound's stability and reactivity. Overall, this compound is of interest in both synthetic and pharmaceutical chemistry due to its versatile reactivity and potential applications.
Formula:C9H13BO3
Synonyms:- Boronicacid, [3-(3-hydroxypropyl)phenyl]- (9CI)
- 3-(3-Hydroxypropyl)benzeneboronicacid
- [3-(3-Hydroxypropyl)phenyl]boronic acid
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Found 3 products.
3-(3-Hydroxypropyl)phenylboronic acid
CAS:Formula:C9H13BO3Purity:98%Color and Shape:SolidMolecular weight:180.00873-(3-Hydroxyprop-1-yl)benzeneboronic acid
CAS:3-(3-Hydroxyprop-1-yl)benzeneboronic acidFormula:C9H13BO3Purity:≥95%Color and Shape: white solidMolecular weight:180.01g/mol


