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.
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
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