264888-37-1

Basic information

• Product Name: 2-tert-butoxycarbonylamino-3-(1-formyl-1H-indol-3-yl)-propionic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester
• Synonyms: 2-tert-butoxycarbonylamino-3-(1-formyl-1H-indol-3-yl)-propionic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester
• CAS NO: 264888-37-1
• Molecular Weight: 628.766
• Mol File: 264888-37-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-tert-butoxycarbonylamino-3-(1-formyl-1H-indol-3-yl)-propionic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-tert-butoxycarbonylamino-3-(1-formyl-1H-indol-3-yl)-propionic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester(264888-37-1)
• EPA Substance Registry System: 2-tert-butoxycarbonylamino-3-(1-formyl-1H-indol-3-yl)-propionic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester(264888-37-1)

Safety Data

• Hazardous Substances Data: 264888-37-1(Hazardous Substances Data)

Upstream product

• 157547-46-1 6-benzyloxy-4,4,5,7-tetramethylhydrocoumarin 
• 100-44-7 benzyl chloride 
• 50442-68-7 6-hydroxy-4,4,5,7-tetramethyl-3,4-dihydrocoumarin 
• 47355-10-2 Nα-tert-butoxycarbonyl-1-formyl-L-tryptophan 
• 157547-47-2 3-(2'-Hydroxy-5'-benzyloxy-4',6'-dimethylphenyl)-3,3-dimethyl-1-propanol 

Downstream Products

• 264888-67-7 2-tert-butoxycarbonylamino-3-(1-formyl-1H-indol-3-yl)-propionic acid 3-(3,6-dihydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester 
• 264888-52-0 2-tert-butoxycarbonylamino-3-(1-formyl-1H-indol-3-yl)-propionic acid 3-(2,4-dimethyl-3,6-dioxo-cyclohexa-1,4-dienyl)-3-methyl-butyl ester 

Relevant articles and documents

A facilitated cyclic ether formation and its potential application in solid-phase peptide and organic synthesis

A 'trimethyl lock' system has been known to facilitate lactonization reactions through what has been termed a stereopopulation control mechanism. We have found that a similar trimethyl lock system can also facilitate cyclic ether formation with the concom