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CAS 369623-85-8

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(3S,4R)-4-amino-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid

Description:
(3S,4R)-4-amino-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid is a chiral amino acid derivative characterized by its pyrrolidine ring structure, which contributes to its unique stereochemistry. The presence of the tert-butoxycarbonyl (Boc) group provides protection for the amino group, making it useful in peptide synthesis and other organic reactions. This compound features both an amino group and a carboxylic acid group, which allows it to participate in various chemical reactions, including coupling reactions to form peptides. Its specific stereochemistry, denoted by the (3S,4R) configuration, is crucial for its biological activity and interactions, particularly in the context of drug design and development. The compound is typically used in research and pharmaceutical applications, particularly in the synthesis of biologically active molecules. As with many amino acid derivatives, it is important to handle this substance with care, following appropriate safety protocols, due to its potential reactivity and biological implications.
Formula:C10H18N2O4
InChI:InChI=1/C10H18N2O4/c1-10(2,3)16-9(15)12-4-6(8(13)14)7(11)5-12/h6-7H,4-5,11H2,1-3H3,(H,13,14)/t6-,7-/m0/s1
SMILES:CC(C)(C)OC(=O)N1C[C@@H]([C@H](C1)N)C(=O)O
Synonyms:
  • (3S,4R)-4-Amino-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester
  • (3S,4R)-4-amino-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-3-carboxylic acid
  • (3S,4R)-4-Amino-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid
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