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CAS 14559-88-7

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2,2-DIMETHYLETHENYLBORONIC ACID

Description:
2,2-Dimethylethenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a dimethyl-substituted ethenyl moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its reactivity, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile building block in organic synthesis, especially in the formation of carbon-carbon bonds. The boronic acid group allows for the formation of stable complexes with diols, making it useful in various applications, including sensor technology and drug development. Additionally, 2,2-dimethylethenylboronic acid exhibits moderate solubility in organic solvents, which facilitates its use in synthetic procedures. Safety precautions should be taken when handling this compound, as boronic acids can be irritants and may pose environmental hazards. Overall, its unique structure and reactivity make it a valuable compound in the field of organic chemistry.
Formula:C4H9BO2
InChI:InChI=1/C4H9BO2/c1-4(2)3-5(6)7/h3,6-7H,1-2H3
SMILES:CC(=CB(O)O)C
Synonyms:
  • Rarechem Ah Pb 0256
  • (2-Methylprop-1-En-1-Yl)Boronic Acid
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