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CAS 90555-65-0

:

(3-ethylphenyl)boronic acid

Description:
(3-Ethylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has an ethyl substituent at the meta position. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents such as ethanol and methanol. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki-Miyaura cross-coupling reactions. The boronic acid group allows for the formation of stable complexes with carbohydrates and other biomolecules, which is valuable in biochemical research. Additionally, (3-ethylphenyl)boronic acid can serve as a building block in the synthesis of more complex organic molecules. Safety considerations include handling it with care, as boronic acids can be irritants and should be used in a well-ventilated area with appropriate personal protective equipment.
Formula:C8H11BO2
InChI:InChI=1/C8H11BO2/c1-2-7-4-3-5-8(6-7)9(10)11/h3-6,10-11H,2H2,1H3
SMILES:CCc1cccc(c1)B(O)O
Synonyms:
  • Boronic acid, B-(3-ethylphenyl)-
  • 3-Ethylphenylboronicacid
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