53017-51-9

Basic information

• Product Name: 5-benzyloxy-N_b-acetyl-L-tryptophan
• CAS NO: 53017-51-9
• Molecular Weight: 352.39
• Mol File: 53017-51-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-benzyloxy-N_b-acetyl-L-tryptophan(CAS DataBase Reference)
• NIST Chemistry Reference: 5-benzyloxy-N_b-acetyl-L-tryptophan(53017-51-9)
• EPA Substance Registry System: 5-benzyloxy-N_b-acetyl-L-tryptophan(53017-51-9)

Safety Data

• Hazardous Substances Data: 53017-51-9(Hazardous Substances Data)

Upstream product

• 85391-99-7 acetylamino-(5-benzyloxy-indol-3-ylmethyl)-malonic acid 
• 68-95-1 (S)-acetylproline 
• 147-85-3 L-proline 
• 154005-67-1 (S)-1-Acetyl-5-hydroxy-pyrrolidine-2-carboxylic acid methyl ester 
• 2311-25-3 N-acetyl-L-proline methyl ester 
• 53017-44-0 5-benzyloxy-N_b-acetyl-L-tryptophan methyl ester 
• 50469-23-3 acetylamino-(5-benzyloxy-indol-3-ylmethyl)-malonic acid diethyl ester 
• 1453-97-0 5-benzyloxygramine 
• 108-24-7 acetic anhydride 

Downstream Products

• 56-69-9 5-hydroxy-L-tryptophan 
• 67010-10-0 N-acetyl-5-hydroxy-L-tryptophan 

Relevant articles and documents

Syntheses of Substituted L- and D-Tryptophans

Several 5-substituted nb-methoxycarbonyl-L- and -D-tryptophan derivatives were synthesized from proline by a new route involving electrochemical oxidation, as well as by the known procedures.Removal of the Nb-methoxycarbonyl group was accomplished by treatment with Me3SiI in refluxing chloroform, then alkaline hydrolysis of the methyl esters afforded 5-substituted L- and D-tryptophans with high optical purities.Keywords - L-tryptophan 5-substituted; D-tryptophan 5-substituted; anodic oxidation; N-methoxycarbonyl group deprotection; Fischer indole synthesis; iodotrimethylsilane