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CAS 21307-97-1

:

(R)-2-benzylsuccinic acid

Description:
(R)-2-benzylsuccinic acid is an organic compound characterized by its chiral structure, which includes a benzyl group attached to the second carbon of a succinic acid backbone. This compound is a member of the class of dicarboxylic acids, featuring two carboxylic acid functional groups (-COOH) that contribute to its acidity and reactivity. The presence of the benzyl group enhances its hydrophobic characteristics, influencing its solubility in organic solvents compared to water. (R)-2-benzylsuccinic acid is known for its potential applications in asymmetric synthesis and as a chiral building block in organic chemistry. Its stereochemistry plays a crucial role in determining its biological activity and interactions with other molecules. The compound is typically synthesized through various methods, including asymmetric synthesis techniques. As with many organic acids, it can participate in various chemical reactions, such as esterification and amidation, making it valuable in the development of pharmaceuticals and fine chemicals. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C11H12O4
InChI:InChI=1/C11H12O4/c12-10(13)7-9(11(14)15)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,12,13)(H,14,15)/t9-/m1/s1
SMILES:c1ccc(cc1)C[C@H](CC(=O)O)C(=O)O
Synonyms:
  • (2R)-2-Benzylsuccinic acid
  • butanedioic acid, 2-(phenylmethyl)-, (2R)-
  • (2R)-2-benzylbutanedioic acid
  • R(+)-Benzylsuccinate
  • Mitiglinide Impurity D
  • (R)-2-BENZYLSUCCINIC ACID / 21307-97-1
  • Mitiglinide Impurity 7
  • (R)-2-Benzylsuccinic acid
  • (2R)-2-(Phenylmethyl)butanedioic acid
  • (R)-2-Benzylbutanedioic acid
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