CymitQuimica logo

CAS 225918-60-5

:

(S)-N-Boc-(2'-chlorophenyl)glycine

Description:
(S)-N-Boc-(2'-chlorophenyl)glycine is a chiral amino acid derivative characterized by its specific stereochemistry and functional groups. The "N-Boc" (tert-butoxycarbonyl) group serves as a protecting group for the amine, facilitating its use in peptide synthesis and other organic reactions. The presence of the 2'-chlorophenyl group indicates that the compound has a chlorinated aromatic ring, which can influence its reactivity and biological activity. This compound is typically used in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. Its chirality is significant in drug design, as the (S)-enantiomer may exhibit different pharmacological properties compared to its (R)-counterpart. The compound is generally stable under standard laboratory conditions but should be handled with care due to the presence of the chlorinated aromatic moiety, which may pose environmental and health risks. Overall, (S)-N-Boc-(2'-chlorophenyl)glycine is a valuable intermediate in organic synthesis, particularly in the field of medicinal chemistry.
Formula:C13H16ClNO4
InChI:InChI=1/C13H16ClNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-6-4-5-7-9(8)14/h4-7,10H,1-3H3,(H,15,18)(H,16,17)/t10-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](c1ccccc1Cl)C(=O)O)O
Synonyms:
  • (2S)-[(tert-Butoxycarbonyl)amino](2-chlorophenyl)acetic acid
  • Benzeneacetic acid, 2-chloro-alpha-[[(1,1-dimethylethoxy)carbonyl]amino]-, (alphaS)-
  • (2S)-[(tert-butoxycarbonyl)amino](2-chlorophenyl)ethanoic acid
  • (2R)-[(tert-butoxycarbonyl)amino](2-chlorophenyl)ethanoic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.