CAS 1236189-95-9: B-[3-(3-Methylbutoxy)phenyl]boronic acid

Description: B-[3-(3-Methylbutoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a 3-methylbutoxy 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 presence of the bulky 3-methylbutoxy group can influence its solubility and reactivity, potentially enhancing its selectivity in chemical reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The compound's structure suggests it may also have potential applications in materials science and as a ligand in coordination chemistry. Overall, B-[3-(3-Methylbutoxy)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.

Formula: C₁₁H₁₇BO₃

InChI: InChI=1S/C11H17BO3/c1-9(2)6-7-15-11-5-3-4-10(8-11)12(13)14/h3-5,8-9,13-14H,6-7H2,1-2H3

InChI key: InChIKey=AIFBGNPSZLRGLB-UHFFFAOYSA-N

SMILES: OB(O)C=1C=CC=C(OCCC(C)C)C1

Synonyms:

• [3-(3-Methylbutoxy)phenyl]boronic acid
• B-[3-(3-Methylbutoxy)phenyl]boronic acid
• Boronic acid, B-[3-(3-methylbutoxy)phenyl]-

[3-(3-Methylbutoxy)phenyl]boronic acid

CAS: 1236189-95-9

Versatile small molecule scaffold

• Formula: C₁₁H₁₇BO₃
• Purity: Min. 95%
• Molecular weight: 208.06 g/mol

[3-(3-methylbutoxy)phenyl]boronic acid

CAS: 1236189-95-9

• Purity: 95%
• Molecular weight: 208.05999755859375