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CAS 209525-73-5

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N-Boc-2-(4'-chlorophenyl)-DL-glycine

Description:
N-Boc-2-(4'-chlorophenyl)-DL-glycine is a chemical compound characterized by its structure, which includes a Boc (tert-butyloxycarbonyl) protecting group attached to the amino group of glycine, along with a 4-chlorophenyl substituent at the second carbon. This compound is typically used in organic synthesis and peptide chemistry, particularly for the protection of amino acids during the synthesis of peptides. The presence of the Boc group enhances the stability of the amino group under various reaction conditions, allowing for selective reactions to occur at other functional groups. The 4-chlorophenyl moiety contributes to the compound's hydrophobic characteristics, influencing its solubility and reactivity. N-Boc-2-(4'-chlorophenyl)-DL-glycine is often utilized in the development of pharmaceuticals and biologically active compounds due to its structural features that can facilitate interactions with biological targets. As with many chemical substances, proper handling and safety precautions are essential, given its potential reactivity and the presence of chlorine in its structure.
Formula:C13H16ClNO4
InChI:InChI=1/C13H16ClNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-4-6-9(14)7-5-8/h4-7,10H,1-3H3,(H,15,18)(H,16,17)
SMILES:CC(C)(C)OC(=NC(c1ccc(cc1)Cl)C(=O)O)O
Synonyms:
  • N-Boc-amino-(4-chlorophenyl)acetic acid
  • tert-Butoxycarbonylamino(4-chlorophenyl)acetic acid
  • [(Tert-Butoxycarbonyl)Amino](4-Chlorophenyl)Acetic Acid
  • N-Boc-amino-(4-chlorophenyl)aceticacid
  • N-Boc-2-(4''-chlorophenyl)-DL-glycine
  • N-Boc-RS-4-Chlorophenylglycine
  • Boc-RS-4-Chlorophenylglycine
  • 4-Chloro-a-(Boc-aMino)-benzeneacetic acid
  • Benzeneacetic acid, 4-chloro-α-[[(1,1-dimethylethoxy)carbonyl]amino]-
  • 2-(4-chlorophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
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