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CAS 1251021-43-8

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Racemic-(3aS,4R,7aS)-2-(tert-butoxycarbonyl)octahydro-1H-isoindole-4-carboxylic acid

Description:
Racemic-(3aS,4R,7aS)-2-(tert-butoxycarbonyl)octahydro-1H-isoindole-4-carboxylic acid is a chiral compound characterized by its complex bicyclic structure, which includes an isoindole moiety. This substance features a tert-butoxycarbonyl (Boc) protecting group, commonly used in organic synthesis to protect amines during reactions. The presence of multiple stereocenters contributes to its racemic nature, indicating that it exists as a mixture of two enantiomers. The octahydro framework suggests that the compound is saturated, which may influence its reactivity and solubility. Typically, compounds like this are of interest in pharmaceutical chemistry due to their potential biological activity, particularly in drug development. The carboxylic acid functional group is significant for its ability to participate in various chemical reactions, including esterification and amidation. Overall, this compound exemplifies the complexity and diversity of organic molecules used in medicinal chemistry and highlights the importance of stereochemistry in determining the properties and activities of chemical substances.
Formula:C14H23NO4
Synonyms:
  • (3aS,4R,7aS)-2-[(2-methylpropan-2-yl)oxycarbonyl]-1,3,3a,4,5,6,7,7a-octahydroisoindole-4-carboxylic acid
  • Racemic-(3aS,4R,7aS)-2-(tert-butoxycarbonyl)octahydro-1H-isoindole-4-carboxylic acid(WX110056)
  • (3aS,4R,7aS)-2-(tert-Butoxycarbonyl)octahydro-1H-isoindole-4-carboxylic acid
  • Racemic-(3aS,4R,7aS)-2-(tert-butoxycarbonyl)octahydro-1H-isoindole-4-carboxylic acid
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