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CAS 183677-71-6

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4-Bromobenzeneboronic acid neopentyl glycol cyclic ester

Description:
4-Bromobenzeneboronic acid neopentyl glycol cyclic ester is a chemical compound characterized by its boronic acid functionality, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. The presence of the bromobenzene moiety contributes to its reactivity and potential for substitution reactions. This compound features a cyclic ester structure, which can enhance its stability and solubility in organic solvents. Additionally, the neopentyl glycol component provides steric hindrance, influencing the compound's reactivity and interactions with other molecules. The compound's boronic acid group is particularly valuable in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. Overall, 4-Bromobenzeneboronic acid neopentyl glycol cyclic ester is a versatile intermediate in the synthesis of complex organic molecules, with applications in pharmaceuticals and materials science. Its unique structural features make it a subject of interest in ongoing research within the field of organic chemistry.
Formula:C11H14BBrO2
InChI:InChI=1/C11H14BBrO2/c1-11(2)7-14-12(15-8-11)9-3-5-10(13)6-4-9/h3-6H,7-8H2,1-2H3
SMILES:CC1(C)COB(c2ccc(cc2)Br)OC1
Synonyms:
  • 2-(4-Bromophenyl)-5,5-dimethyl-1,3,2-dioxaborinane
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