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CAS 913835-82-2

:

Benzenepropanoic acid, 3-borono-, α-ethyl ester

Description:
Benzenepropanoic acid, 3-borono-, α-ethyl ester, with the CAS number 913835-82-2, is an organic compound that features a boronic acid moiety attached to a benzenepropanoic acid structure. This compound typically exhibits characteristics common to boronic esters, 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 ethyl ester group contributes to its solubility in organic solvents and may influence its reactivity and stability. The compound is likely to be a white to off-white solid or a viscous liquid, depending on its purity and specific conditions. Its chemical properties may include moderate polarity, and it may participate in reactions typical of both carboxylic acids and boronic acids, such as Suzuki coupling reactions. Overall, this compound is of interest in the development of pharmaceuticals and materials science due to its unique structural features and reactivity.
Formula:C11H15BO4
InChI:InChI=1S/C11H15BO4/c1-2-16-11(13)7-6-9-4-3-5-10(8-9)12(14)15/h3-5,8,14-15H,2,6-7H2,1H3
InChI key:InChIKey=RTJGTDXOUMFFRS-UHFFFAOYSA-N
SMILES:C(CC(OCC)=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • 3-(2-Ethoxycarbonylethyl)Benzeneboronic Acid 97
  • Benzenepropanoic acid, 3-borono-, α-ethyl ester
  • [3-(2-Ethoxycarbonylethyl)phenyl]boronic acid
  • [3-(3-Ethoxy-3-oxopropyl)phenyl]boronic acid
  • ETHYL 3-(3-BORONOPHENYL)PROPIONATE
  • (3-(3-ethoxy-3-oxopropyL
  • 3-(3-ETHOXY-3-OXOPROPYL)PHENYLBORONIC ACID
  • (3-(3-Ethoxy-3-oxopropyl)phenyl)boronicaci
  • 3-(2-ETHOXYCARBONYLETHYL)PHENYLBORONIC ACID
  • 3-[2-(Ethoxycarbonyl)ethyl]benzeneboronic acid 97%
  • 3-(2-ETHOXYCARBONYLETHYL)BENZENEBORONIC ACID
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