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CAS 874288-38-7

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[4-(ethoxycarbonyl)-3-fluorophenyl]boronic acid

Description:
[4-(Ethoxycarbonyl)-3-fluorophenyl]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 organic synthesis applications, particularly in cross-coupling reactions. The compound features a fluorinated aromatic ring, which can influence its electronic properties and reactivity. The ethoxycarbonyl group contributes to its solubility and stability, enhancing its utility in synthetic chemistry. This compound is typically used in the development of pharmaceuticals and agrochemicals, as well as in materials science for the synthesis of polymers and other advanced materials. Its boronic acid functionality allows for participation in Suzuki-Miyaura coupling reactions, facilitating the formation of carbon-carbon bonds. Overall, [4-(ethoxycarbonyl)-3-fluorophenyl]boronic acid is a versatile building block in organic synthesis, with applications spanning various fields of chemistry.
Formula:C9H10BFO4
InChI:InChI=1/C9H10BFO4/c1-2-15-9(12)7-4-3-6(10(13)14)5-8(7)11/h3-5,13-14H,2H2,1H3
SMILES:CCOC(=O)c1ccc(cc1F)B(O)O
Synonyms:
  • Benzoic acid, 4-borono-2-fluoro-, ethyl ester
  • [4-(Ethoxycarbonyl)-3-fluorophenyl]boronic acid
  • 4-(ETHOXYCARBONYL)-3-FLUOROBENZENEBORONIC ACID
  • 4-ETHOXYCARBONYL-3-FLUOROPHENYLBORONIC ACID
  • 4-(Ethoxycarbonyl)-3-fluorobenzeneboronic acid 95%
  • 4-(Ethoxycarbonyl)-3-fluorobenzeneboronicacid95%
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