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Boc-D-Trp(1-Me)-OH

Boc-D-Trp(1-Me)-OH combines a protecting group with a methylated indole ring, offering steric and electronic modulation for synthesis. The D-configuration contributes to altered chiral recognition during coupling reactions. The compound is widely used in constructing conformationally restricted peptides. Its chemical profile supports advanced strategy development in peptide synthesis.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: HB00072

CAS No:103943-63-1

Synonyms/Alias:103943-63-1;Boc-D-Trp(Me)-OH;N-Boc-1-methyl-D-tryptophan;(R)-2-(tert-butoxycarbonylamino)-3-(1-methyl-1H-indol-3-yl)propanoic acid;(2R)-3-(1-methylindol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid;(R)-2-((tert-Butoxycarbonyl)amino)-3-(1-methyl-1H-indol-3-yl)propanoic acid;Na-(tert-Butoxycarbonyl)-1-methyl-D-tryptophan;(2R)-2-[(tert-butoxycarbonyl)amino]-3-(1-methylindol-3-yl)propanoic acid;Boc-D-Trp(CH3)-OH;SCHEMBL2837978;OHPBREBKPBFZCY-CYBMUJFWSA-N;AS-82357;N-tert-butoxycarbonyl-1-methyl-D-tryptophan;CS-0106457;F80802;N-(tert-butoxycarbonyl)-1-methyl-D-tryptophan;Nalpha-tert-butyloxycarbonyl-1-methyl-D-tryptophan;(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(1-methyl-1H-indol-3-yl)propanoic acid;(R)-2-(tert-butoxycarbonylamino)-3-(1-methyl-1H-indol-3-yl)propanoic Acid

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C17H22N2O4
M.W/Mr.
318.36758
Sequence
Three Letter Code:Boc-D-Trp(Me)-OH
Purity
98%

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