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CAS 261904-39-6

:

(2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid

Description:
(2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid is an organic compound characterized by its chiral center, which contributes to its specific stereochemistry. This compound features a bromine atom and a hydroxyl group attached to a branched propanoic acid backbone, making it a bromo-hydroxy acid. The presence of the bromine atom introduces unique reactivity, allowing for potential applications in organic synthesis and medicinal chemistry. The hydroxyl group enhances its solubility in polar solvents and can participate in hydrogen bonding, influencing its physical properties and reactivity. As a carboxylic acid, it exhibits acidic behavior, capable of donating a proton in solution. Its chirality may also affect its biological activity, making it of interest in pharmaceutical research. The compound's molecular structure suggests it could be involved in various chemical reactions, including substitution and esterification. Overall, (2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid is a versatile compound with potential applications in both synthetic and biological chemistry.
Formula:C4H7BrO3
InChI:InChI=1/C4H7BrO3/c1-4(8,2-5)3(6)7/h8H,2H2,1H3,(H,6,7)/t4-/m0/s1
SMILES:C[C@](CBr)(C(=O)O)O
Synonyms:
  • (2R)-3-Bromo-2-hydroxy-2-methylpropionic acid
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