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CAS 47355-10-2

:

N(alpha)-boc-N(in)-formyl-L-tryptophan

Description:
N(alpha)-Boc-N(in)-formyl-L-tryptophan is a derivative of the amino acid tryptophan, characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group at the alpha-amino group and a formyl group at the indole nitrogen. This compound is typically used in peptide synthesis and as an intermediate in the preparation of more complex molecules. The Boc group serves to protect the amino group during chemical reactions, allowing for selective modifications of other functional groups. The formyl group introduces a reactive aldehyde functionality, which can participate in various chemical reactions, including condensation and cyclization. This compound is generally stable under standard laboratory conditions but may be sensitive to moisture and heat. Its solubility is typically in organic solvents, making it suitable for use in organic synthesis. As with many amino acid derivatives, it may exhibit biological activity, and its derivatives can be explored for potential pharmaceutical applications. Proper handling and storage conditions are essential to maintain its integrity and reactivity.
Formula:C17H20N2O5
InChI:InChI=1/C17H20N2O5/c1-17(2,3)24-16(23)18-13(15(21)22)8-11-9-19(10-20)14-7-5-4-6-12(11)14/h4-7,9-10,13H,8H2,1-3H3,(H,18,23)(H,21,22)/t13-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1cn(C=O)c2ccccc12)C(=O)O)O
Synonyms:
  • na-T-boc-N-in-formyl-L-tryptophan
  • Boc-Trp(For)-OH
  • Boc-Trp(CHO)-OH
  • N-alpha-t-butyloxycabonyl-N-formyl-L-tryptophane
  • N alpha-(tert-Butoxycarbonyl)-N1-formyl-L-tryptophan
  • N-(tert-butoxycarbonyl)-1-formyl-L-tryptophan
  • N-α-Boc-N-in-formyl-L-tryptophan
  • (Tert-Butoxy)Carbonyl Trp(For)-OH
  • N-ALPHA-T-BOC-N-FORMYL-L-TRYPTOPHAN
  • BOC-TRP(FOR)-OH USP/EP/BP
  • See more synonyms
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