603121-75-1

Basic information

• Product Name: 3-(3-chlorophenyl)-N-[(1S)-2-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-1-methyl-2-oxoethyl]-N-methyl-2-oxopropanamide
• Synonyms: 3-(3-chlorophenyl)-N-[(1S)-2-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-1-methyl-2-oxoethyl]-N-methyl-2-oxopropanamide
• CAS NO: 603121-75-1
• Molecular Weight: 446.931
• Mol File: 603121-75-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(3-chlorophenyl)-N-[(1S)-2-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-1-methyl-2-oxoethyl]-N-methyl-2-oxopropanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-chlorophenyl)-N-[(1S)-2-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-1-methyl-2-oxoethyl]-N-methyl-2-oxopropanamide(603121-75-1)
• EPA Substance Registry System: 3-(3-chlorophenyl)-N-[(1S)-2-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-1-methyl-2-oxoethyl]-N-methyl-2-oxopropanamide(603121-75-1)

Safety Data

• Hazardous Substances Data: 603121-75-1(Hazardous Substances Data)

Upstream product

• 96406-06-3 3-(3-Chlorphenyl)-2-oxopropansaeure 
• 603121-71-7 (2S)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(methylamino)propanamide 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 603121-67-1 benzyl (1S)-2-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-1-methyl-2-oxoethyl(methyl)carbamate 

Relevant articles and documents

Diastereoselective synthesis of 1-benzyltetrahydroisoquinoline derivatives from amino acids by 1,4 chirality transfer

L-Amino acids (L-Ala, L-Phe, L-Val, L-Pro) were used as a source of chirality in the diastereoselective synthesis of tetrahydroisoquinoline derivatives. The key step was the Pictet-Spengler condensation of ketoamides 4 and 10, which proceeded under very m