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CAS 1218790-94-3

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B-(3-Ethyl-4-formylphenyl)boronic acid

Description:
B-(3-Ethyl-4-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an ethyl group and a formyl group. This compound typically exhibits properties associated with boronic acids, 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 formyl group suggests potential reactivity in condensation reactions, while the ethyl substituent can influence the compound's solubility and steric properties. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's structure may also impart specific optical or electronic properties, making it of interest in materials science. Overall, B-(3-Ethyl-4-formylphenyl)boronic acid is a versatile compound with potential applications in both synthetic and applied chemistry.
Formula:C9H11BO3
InChI:InChI=1S/C9H11BO3/c1-2-7-5-9(10(12)13)4-3-8(7)6-11/h3-6,12-13H,2H2,1H3
InChI key:InChIKey=CUHGCQVNNDUJCQ-UHFFFAOYSA-N
SMILES:C(C)C1=C(C=O)C=CC(B(O)O)=C1
Synonyms:
  • Boronic acid, B-(3-ethyl-4-formylphenyl)-
  • (3-Ethyl-4-formylphenyl)boronicacid
  • 3-Ethyl-4-formylphenylboronic acid
  • (3-Ethyl-4-formylphenyl)boronic acid
  • B-(3-Ethyl-4-formylphenyl)boronic acid
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