123050-52-2

Basic information

• Product Name: trans-2-benzyl-3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole
• Synonyms: trans-2-benzyl-3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole
• CAS NO: 123050-52-2
• Molecular Weight: 396.489
• Mol File: 123050-52-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: trans-2-benzyl-3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole(CAS DataBase Reference)
• NIST Chemistry Reference: trans-2-benzyl-3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole(123050-52-2)
• EPA Substance Registry System: trans-2-benzyl-3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole(123050-52-2)

Safety Data

• Hazardous Substances Data: 123050-52-2(Hazardous Substances Data)

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 73327-10-3 N_b-benzyltriptophan methyl ester 
• 31771-33-2 2-phenyl-4,4,6-trimethyltetrahydro-(2H)-1,3-oxazine 
• 63229-68-5 methyl N-benzyl-L-tryptophanate 
• 100-52-7 benzaldehyde 

Downstream Products

• 50302-60-8 cis-(3-(methoxycarbonyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indol-1-yl)benzene 
• 50302-61-9 trans-(3-(methoxycarbonyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indol-1-yl)benzene 

Relevant articles and documents

A versatile approach to trans-1,3-disubstituted tetrahydro-β-carbolines using oxazinanes

Under the conditions of thermodynamic control, the diastereoselectivity of the reaction between tryptophan esters and oxazinanes (carbonyl equivalents) can be controlled by incorporating N(b)-benzyl substituents; the reaction proceeds in essentially quant

Pictet-Spengler reactions in aprotic media. Stereospecificity in the Pictet-Spengler reaction

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