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CAS 871125-79-0

:

B-[3-Formyl-5-(1-methylethoxy)phenyl]boronic acid

Description:
B-[3-Formyl-5-(1-methylethoxy)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 phenyl ring substituted with a formyl group and an ethoxy group, contributing to its reactivity and solubility properties. The presence of the formyl group indicates potential for further functionalization, while the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling. This compound may exhibit moderate to high polarity due to the functional groups, influencing its solubility in polar solvents. Additionally, boronic acids are often sensitive to moisture and can undergo hydrolysis, which is an important consideration in handling and storage. Overall, B-[3-Formyl-5-(1-methylethoxy)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry and materials science.
Formula:C10H13BO4
InChI:InChI=1S/C10H13BO4/c1-7(2)15-10-4-8(6-12)3-9(5-10)11(13)14/h3-7,13-14H,1-2H3
InChI key:InChIKey=TYKYVLDAFDKFHV-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=CC(B(O)O)=CC(C=O)=C1
Synonyms:
  • 3-Formyl-5-isopropoxyphenylboronic acid
  • [3-Formyl-5-(propan-2-yloxy)phenyl]boronic acid
  • B-[3-Formyl-5-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, [3-formyl-5-(1-methylethoxy)phenyl]-
  • Boronic acid, B-[3-formyl-5-(1-methylethoxy)phenyl]-
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