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CAS 1072952-00-1

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B-[3-Formyl-4-(1-methylethoxy)phenyl]boronic acid

Description:
B-[3-Formyl-4-(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 Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds. This compound may exhibit properties such as moderate solubility in organic solvents and potential reactivity with biological targets, making it of interest in drug development and materials science. Its specific characteristics, such as melting point, boiling point, and spectral data, would typically be determined through experimental methods and may vary based on purity and environmental conditions.
Formula:C10H13BO4
InChI:InChI=1S/C10H13BO4/c1-7(2)15-10-4-3-9(11(13)14)5-8(10)6-12/h3-7,13-14H,1-2H3
InChI key:InChIKey=MFWMHBLPARKSLU-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(C=O)C=C(B(O)O)C=C1
Synonyms:
  • B-[3-Formyl-4-(1-methylethoxy)phenyl]boronic acid
  • (3-Formyl-4-isopropoxyphenyl)boronic acid
  • Boronic acid, B-[3-formyl-4-(1-methylethoxy)phenyl]-
  • 3-Formyl-4-isopropoxyphenylboronic acid
  • [3-Formyl-4-(propan-2-yloxy)phenyl]boronic acid
  • [3-Formyl-4-(1-methylethoxy)phenyl]boronic acid
  • 3-Formyl-4-isopropoxyphenylboronic acid (contains varying amounts of Anhydride)
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