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CAS 114525-81-4

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(R)-4-Boc-Thiomorpholine-3-Carboxylic Acid

Description:
(R)-4-Boc-Thiomorpholine-3-Carboxylic Acid is a chiral compound characterized by its thiomorpholine ring structure, which incorporates a sulfur atom into a six-membered ring. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amine functionality, enhancing the compound's stability and facilitating its use in various synthetic applications. This compound is typically utilized in the synthesis of peptides and other bioactive molecules due to its ability to introduce chirality and functional diversity. The presence of the carboxylic acid group contributes to its acidic properties, making it soluble in polar solvents. Additionally, the stereochemistry indicated by the "(R)" designation suggests that it possesses specific spatial arrangements that can influence its biological activity and interactions. Overall, (R)-4-Boc-Thiomorpholine-3-Carboxylic Acid is valued in medicinal chemistry and organic synthesis for its unique structural features and reactivity.
Formula:C10H17NO4S
InChI:InChI=1/C10H17NO4S/c1-10(2,3)15-9(14)11-4-5-16-6-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)
SMILES:CC(C)(C)OC(=O)N1CCSCC1C(=O)O
Synonyms:
  • (R)-4-(Tert-Butoxycarbonyl)-Thiomorpholine-3-Carboxylic Acid
  • (R)-Boc-3-Carboxythiomorpholine
  • (3R)-4-(Tert-Butoxycarbonyl)Thiomorpholine-3-Carboxylic Acid
  • 4-(Tert-Butoxycarbonyl)Thiomorpholine-3-Carboxylic Acid
  • (R)-N-Boc-Thiomorpholine-3-Carboxylic Acid
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