171280-99-2

Basic information

• Product Name: (2S)-2-amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-3-methylbutanamide
• Synonyms: (2S)-2-amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-3-methylbutanamide
• CAS NO: 171280-99-2
• Molecular Weight: 280.367
• Mol File: 171280-99-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S)-2-amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-3-methylbutanamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2-amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-3-methylbutanamide(171280-99-2)
• EPA Substance Registry System: (2S)-2-amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-3-methylbutanamide(171280-99-2)

Safety Data

• Hazardous Substances Data: 171280-99-2(Hazardous Substances Data)

Upstream product

• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 2816-12-8 4-isopropyl-2,5-oxazolidinedione 
• 143440-09-9 (S)-2-[(1,1-dimethylethyl)-oxycarbonyl]-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)]-ethyl-amide 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 
• 143491-22-9 benzyl (1S)-1-({[2-(3,4-dimethoxyphenyl)ethyl]amino}carbonyl)-2-methylpropylcarbamate 

Downstream Products

• 174601-20-8 (S)-2-(N,N-dimethylsulfamoyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxy-phenyl)-ethyl]-amide 

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

Microbicides

α-Amino acid amides of the formula I STR1 in which n is the number zero or one; R1 is C1 -C12 alkyl, which is unsubstituted or can be substituted by C1 -C4 alkoxy, C1 -C4 alkylth