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CAS 58521-49-6

:

(3S,4S)-N-boc-4-amino-3-hydroxy-6-methyl heptanoic acid

Description:
(3S,4S)-N-boc-4-amino-3-hydroxy-6-methyl heptanoic acid is a chiral amino acid derivative characterized by its specific stereochemistry and functional groups. The "N-boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group, which is commonly used in peptide synthesis to protect amines. The compound features a heptanoic acid backbone, which consists of a seven-carbon chain, with a hydroxyl group at the 3-position and an amino group at the 4-position, contributing to its biological activity. The presence of a methyl group at the 6-position adds to its structural complexity. This compound is typically utilized in the synthesis of peptides and other bioactive molecules due to its ability to participate in various chemical reactions while maintaining the integrity of the functional groups. Its chirality is significant in pharmaceutical applications, as the specific stereoisomer can influence the biological activity and interaction with biological targets. Overall, this compound is valuable in medicinal chemistry and biochemistry for its potential therapeutic applications.
Formula:C13H25NO5
InChI:InChI=1/C13H25NO5/c1-8(2)6-9(10(15)7-11(16)17)14-12(18)19-13(3,4)5/h8-10,15H,6-7H2,1-5H3,(H,14,18)(H,16,17)/t9-,10+/m1/s1
Synonyms:
  • (3S,4S)-4-(Boc-amino)-3-hydroxy-6-methyl-heptanoic acid
  • Boc-statine
  • (3S,4S)-4-(N-tert-butoxycarbonyl)amino-3-hydroxy-6-methylheptanoic acid
  • N-tert-butoxycarbonyl statine
  • Boc-Sta-OH
  • Boc-(3S,4S)Sta-OH
  • Boc-Sta(3S,4S)-OH
  • (3S,4R)-4-[(tert-butoxycarbonyl)amino]-3-hydroxy-6-methylheptanoic acid
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