72156-62-8

Basic information

• Product Name: BOC-TRP-PHE-OME
• Synonyms: BOC-TRP-PHE-OME;N-[(1,1-Dimethylethoxy)Carbonyl]-L-Tryptophyl-L-Phenylalanine Methyl Ester;N-[N-[(1,1-Dimethylethoxy)carbonyl]-L-tryptophyl]-L-phenylalanine methyl ester;Boc-Trp-Phe-OMe≥ 98% (HPLC);(Tert-Butoxy)Carbonyl Trp-Phe-OMe
• CAS NO: 72156-62-8
• Molecular Formula: C₂₆H₃₁N₃O₅
• Molecular Weight: 465.54
• Mol File: 72156-62-8.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 706.7 °C at 760 mmHg
• Flash Point: 381.2 °C
• Appearance: /
• Density: 1.215 g/cm³
• Vapor Pressure: 8.03E-20mmHg at 25°C
• Refractive Index: 1.591
• Storage Temp.: Store at 0°C
• CAS DataBase Reference: BOC-TRP-PHE-OME(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-TRP-PHE-OME(72156-62-8)
• EPA Substance Registry System: BOC-TRP-PHE-OME(72156-62-8)

Safety Data

• Hazardous Substances Data: 72156-62-8(Hazardous Substances Data)

Usage

Chemical Properties

White powder

InChI:InChI=1/C26H31N3O5/c1-26(2,3)34-25(32)29-21(15-18-16-27-20-13-9-8-12-19(18)20)23(30)28-22(24(31)33-4)14-17-10-6-5-7-11-17/h5-13,16,21-22,27H,14-15H2,1-4H3,(H,28,30)(H,29,32)

Upstream product

• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 13139-14-5 Boc-Trp-OH 
• 3392-11-8 2,5-dioxopyrrolidin-1-yl N-(tert-butoxycarbonyl)-L-tryptophanate 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 

Downstream Products

• 1053209-09-8 (N-tert-butoxycarbonyl-1-carbobenzyloxy-L-tryptophanyl)-L-phenylalanine methyl ester 
• 1233078-23-3 diethyl 2-(3-((S)-2-((tert-butoxycarbonyl)amino)-3-(((S)-1-methoxy-1-oxo-3-phenylpropan-2-yl)amino)-3-oxopropyl)-1H-indol-2-yl)malonate 
• 1227608-37-8 C₃₂H₃₅IN₄O₅ 
• 34337-45-6 Boc-Trp-Phe-OH 
• 870622-79-0 C₇₃H₈₄N₈O₁₄ 
• 808771-91-7 2-[2-[2-{2-[2-[2-tert-butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-yl)-propionylamino]-3-phenyl-propionylamino}-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-yl)-propionylamino]-3-phenyl-propionic acid methyl ester 
• 808771-72-4 2-[2-[2-tert-butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-yl)-propionylamino]-3-phenyl-propionic acid methyl ester 

Relevant articles and documents

Synthesis, characterization, and DNA binding and cleavage properties of copper(II)-tryptophanphenylalanine-1,10-phenanthroline/2,2′-bipyridine complexes

The mononuclear dipeptide-based CuII complexes [Cu II(trp-phe)(phen)(H2O)] ClO4 (1) and [CuII(trp-phe)(bpy)(H2O)] ClO4 (2) (trp-phe=tryptophanphenylalanine, phen=1,10-phenanthrol

Late-stage construction of stapled peptides through Fujiwara-Moritani reaction between tryptophan and olefins

Herein, the first example of a palladium-catalyzed Fujiwara-Moritani reaction for olefination of tryptophan (Trp) residues, free from directing groups, was presented. The developed reaction proceeds efficiently for peptide modification, ligation and pepti

Solid-State Radical C?H Trifluoromethylation Reactions Using Ball Milling and Piezoelectric Materials

The application of piezoelectricity for the generation of trifluoromethyl (CF3) radicals is reported together with the development of a method for the mechanochemical C?H trifluoromethylation of aromatic compounds. As compared to conventional solution-based approaches, this mechanoredox C?H trifluoromethylation enables cleaner and more sustainable access to a wide range of trifluoromethylated N-heterocycles and peptides, which are important structural motifs in modern drug discovery. This study thus represents an important milestone for future applications of mechanoredox systems to medicinal and pharmaceutical science.