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CAS 673456-16-1

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2-Bromomethyl-4-fluorophenylboronic acid neopentyl glycol ester

Description:
2-Bromomethyl-4-fluorophenylboronic acid neopentyl glycol ester is a specialized organic 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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a bromomethyl group and a fluorophenyl moiety, which can influence its reactivity and solubility. The neopentyl glycol ester component contributes to the compound's stability and solubility in organic solvents. This compound is typically used in synthetic organic chemistry, especially in the development of pharmaceuticals and agrochemicals, due to its ability to participate in cross-coupling reactions. Its unique structure allows for specific interactions in biological systems, making it a valuable tool in medicinal chemistry. As with many boronic acids, it may exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions to maintain its integrity and reactivity.
Formula:C12H15BBrFO2
InChI:InChI=1/C12H15BBrFO2/c1-12(2)7-16-13(17-8-12)11-4-3-10(15)5-9(11)6-14/h3-5H,6-8H2,1-2H3
SMILES:CC1(C)COB(c2ccc(cc2CBr)F)OC1
Synonyms:
  • 2-[2-(Bromomethyl)-4-Fluoro-Phenyl]-5,5-Dimethyl-1,3,2-Dioxaborinane
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