1108146-41-3

Basic information

• Product Name: (S)-methyl 2-((S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanamido)-3-(1H-indol-3-yl)propanoate
• Synonyms: (S)-methyl 2-((S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanamido)-3-(1H-indol-3-yl)propanoate
• CAS NO: 1108146-41-3
• Molecular Weight: 515.566
• Mol File: 1108146-41-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-methyl 2-((S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanamido)-3-(1H-indol-3-yl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl 2-((S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanamido)-3-(1H-indol-3-yl)propanoate(1108146-41-3)
• EPA Substance Registry System: (S)-methyl 2-((S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanamido)-3-(1H-indol-3-yl)propanoate(1108146-41-3)

Safety Data

• Hazardous Substances Data: 1108146-41-3(Hazardous Substances Data)

Upstream product

• 5545-54-0 N-(benzyloxycarbonyl)-O-(1,1-dimethylethyl)-L-tyrosine 
• 7524-52-9 (S)-tryptophan methyl ester hydrochloride 
• 1164-16-5 Z-L-Tyr-OH 
• 5618-98-4 N-α-benzyloxycarbonyl-DL-tyrosine 

Relevant articles and documents

A conjugate Lewis base-Br?nsted acid catalyst for the sulfenylation of nitrogen containing heterocycles under mild conditions

Catalysts that contain a thiourea tethered to a carboxylic acid were found to affect the sulfenylation of indoles and other N-heterocycles on the hour time scale at room temperature. The mild nature of these conditions allowed for the incorporation of diverse functionalities into more complex heterocycles.

Design, synthesis, and application of enantioselective coupling reagent with a traceless chiral auxiliary

(Chemical Equation Presented) Stable chiral N-triazinylbrucinium tetrafluoroborate enantioselectively activates racemic carboxylic acids yielding enantiomerically enriched amides, esters, and dipeptides with er from 8:92 to 0.5:99.5. Due to the departure