132659-98-4

Basic information

• Product Name: Methyl N-(diphenylmethyl)-D,L-tryptophanate
• CAS NO: 132659-98-4
• Molecular Weight: 384.478
• Mol File: 132659-98-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Methyl N-(diphenylmethyl)-D,L-tryptophanate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl N-(diphenylmethyl)-D,L-tryptophanate(132659-98-4)
• EPA Substance Registry System: Methyl N-(diphenylmethyl)-D,L-tryptophanate(132659-98-4)

Safety Data

• Hazardous Substances Data: 132659-98-4(Hazardous Substances Data)

Upstream product

• 118553-32-5 Methyl N-(diphenylmethylene)-D,L-tryptophanates 
• 120-72-9 indole 
• 118553-21-2 Methyl N-(diphenylmethylene)-α,β-didehydroalaninate 

Downstream Products

• 73327-06-7 trans-1-cyclohexyl-3-(methoxycarbonyl)-1-propyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole 
• 143998-54-3 trans-3-(methoxycarbonyl)-1-methyl-2-(diphenylmethyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole 
• 143998-56-5 trans-3-(methoxycarbonyl)-2-(diphenylmethyl)-1-propyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole 

Relevant articles and documents

Mechanism driven trans stereospecificity in the Pictet-Spengler reaction. Stereospecific formation of trans-1,2,3-trisubstituted-tetrahydro β-carbolines by condensation of N(b)-diphenylmethyl tryptophan isopropyl esters with aldehydes

Stereoelectronic control in the Pictet-Spengler condensation of N(b)-alkylsubstituted tryptophan alkyl esters has been employed to promote 100% stereoselectivity in this process. The reaction of N(b)-diphenylmethyl tryptophan isopropyl ester 8 with acetal