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CAS 957062-87-2

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(2-ethoxycarbonyl-5-fluoro-phenyl)boronic acid

Description:
(2-Ethoxycarbonyl-5-fluoro-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 organic synthesis applications, particularly in cross-coupling reactions like Suzuki coupling. The compound features a phenyl ring substituted with a fluorine atom and an ethoxycarbonyl group, which contributes to its reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in nucleophilic reactions, while the ethoxycarbonyl group can enhance the compound's stability and solubility in organic solvents. This compound is typically used in medicinal chemistry and materials science for the development of pharmaceuticals and advanced materials. Its unique structural features make it a valuable intermediate in the synthesis of more complex organic molecules. Safety and handling precautions should be observed, as with all boronic acids, due to potential reactivity and toxicity.
Formula:C9H10BFO4
InChI:InChI=1/C9H10BFO4/c1-2-15-9(12)7-4-3-6(11)5-8(7)10(13)14/h3-5,13-14H,2H2,1H3
InChI key:InChIKey=DIHBRMAJVXAIOE-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=C(B(O)O)C=C(F)C=C1
Synonyms:
  • Benzoic acid, 2-borono-4-fluoro-, 1-ethyl ester
  • (2-Ethoxycarbonyl-5-fluorophenyl)boronic acid
  • [2-(Ethoxycarbonyl)-5-fluorophenyl]boronic acid
  • 1-Ethyl 2-borono-4-fluorobenzoate
  • 2-Ethoxycarbonyl-5-fluorophenylboronic acid
  • Ethyl 2-borono-4-fluorobenzoate
  • 2-Ethoxycabonyl-5-fluorophenylboronic acid
  • 2-(Ethoxycarbonyl)-5-fluorobenzeneboronic acid
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