Fmoc-7-methyl-DL-tryptophan

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Fmoc-7-methyl-DL-tryptophan

CAT No: CP07680

Synonyms/Alias:Fmoc-7-methyl-DL-tryptophan;138775-53-8;2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(7-methyl-1H-indol-3-yl)propanoic acid;N-Fmoc-7-methyl-DL-tryptophan;2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(7-methyl-1H-indol-3-yl)propanoic acid;2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(7-methyl-1H-indol-3-yl)propanoic acid;SCHEMBL16099975;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(7-methyl-1H-indol-3-yl)propanoic acid;MFCD02682379;AKOS015837415;AS-86023;Fmoc-7-methyl-DL-tryptophan, AldrichCPR;CS-0280153;G87258;EN300-12627949;2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(7-methyl-1H-indol-3-yl)propanoicacid;

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
C27H24N2O4
M.W/Mr.
440.5
Sequence
Three Letter Code:Fmoc-DL-Trp(7-Me)-OH
InChI
InChI=1S/C27H24N2O4/c1-16-7-6-12-18-17(14-28-25(16)18)13-24(26(30)31)29-27(32)33-15-23-21-10-4-2-8-19(21)20-9-3-5-11-22(20)23/h2-12,14,23-24,28H,13,15H2,1H3,(H,29,32)(H,30,31)
InChI Key
LIHWPPTURGLCAT-UHFFFAOYSA-N
References
1. Vallee, MRJ. et al. (2011). Staudinger-Phosphonite Reactions for the Chemoselective Transformation of Azido-Containing Peptides and Proteins. Org Lett 13, 5440.
2. Staudinger, H. & Meyer, J. (1919). Uberneueorganische Phosphorverbindungen III. Phosphinmethylenederivative und Phosphinimine. Helvetica Chim Acta 2, 635.
3. Oh, K-I. et al. (2008). ß-Azidoalanine as an IR Probe: Application to Amyloid Aß (16-22) Aggregation. J Phys Chem B 112, 10352.

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