CAS 2121512-33-0

B-[3-Bromo-5-(pentyloxy)phenyl]boronic acid

Description:

B-[3-Bromo-5-(pentyloxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a bromine atom and a pentyloxy group attached to a phenyl ring, contributing to its unique reactivity and solubility properties. The bromine substituent can facilitate cross-coupling reactions, such as Suzuki-Miyaura coupling, while the pentyloxy group enhances the compound's lipophilicity, potentially improving its bioavailability in pharmaceutical contexts. Additionally, boronic acids are often employed in the development of sensors and in the field of materials science due to their ability to form complexes with carbohydrates. Overall, B-[3-Bromo-5-(pentyloxy)phenyl]boronic acid exhibits a combination of functional groups that make it a versatile compound in chemical research and applications.

Formula: C₁₁H₁₆BBrO₃

InChI: InChI=1S/C11H16BBrO3/c1-2-3-4-5-16-11-7-9(12(14)15)6-10(13)8-11/h6-8,14-15H,2-5H2,1H3

InChI key: InChIKey=FXZSUYTZYXCKPP-UHFFFAOYSA-N

SMILES: B(O)(O)C1=CC(OCCCCC)=CC(Br)=C1

Synonyms:

• B-[3-Bromo-5-(pentyloxy)phenyl]boronic acid
• Boronic acid, B-[3-bromo-5-(pentyloxy)phenyl]-

Boronic acid, B-[3-bromo-5-(pentyloxy)phenyl]-

CAS: 2121512-33-0

Formula: C₁₁H₁₆BBrO₃

Purity: 95%

Molecular weight: 286.9579

Ref: IN-DA01RVOG