250665-95-3

Basic information

• Product Name: 1,2-Hydrazinedicarboxylic acid, 1-[(1S)-2-[[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]methylamino]-2-ox o-1-(3,4,5-trimethoxyphenyl)ethyl]-, bis(1,1-dimethylethyl) ester
• CAS NO: 250665-95-3
• Molecular Formula: C31H45N3O9
• Molecular Weight: 603.713
• Mol File: 250665-95-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-Hydrazinedicarboxylic acid, 1-[(1S)-2-[[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]methylamino]-2-ox o-1-(3,4,5-trimethoxyphenyl)ethyl]-, bis(1,1-dimethylethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Hydrazinedicarboxylic acid, 1-[(1S)-2-[[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]methylamino]-2-ox o-1-(3,4,5-trimethoxyphenyl)ethyl]-, bis(1,1-dimethylethyl) ester(250665-95-3)
• EPA Substance Registry System: 1,2-Hydrazinedicarboxylic acid, 1-[(1S)-2-[[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]methylamino]-2-ox o-1-(3,4,5-trimethoxyphenyl)ethyl]-, bis(1,1-dimethylethyl) ester(250665-95-3)

Safety Data

• Hazardous Substances Data: 250665-95-3(Hazardous Substances Data)

Upstream product

• 16466-61-8 1,2-bis(t-butyloxycarbonyl)hydrazine 
• 247118-51-0 (+)-<1'S,2'S>-N-(2'-hydroxy-1'-methyl-2'-phenylethyl)-N-methyl-2-(3,4,5-trimethoxyphenyl)acetamide 
• 870-50-8 di-tert-butyl-diazodicarboxylate 
• 870-50-8 (Z)-N-[(tert-butoxy)carbonyl]imino(tert-butoxy)formamide 

Downstream Products

• 250665-99-7 [2S,1'S,2'S]-(+)-2-amino-N-(2'-hydroxy-1'-methyl-2'-phenylethyl)-N-methyl-2-(3,4,5-trimethoxyphenyl)acetamide 
• 474126-01-7 (2S)-2-amino-1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethanone 
• 761395-52-2 (1R,2S)-(-)-2-amino-1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethanol 
• 58716-92-0 (2S)-(+)-3,4,5-trimethoxyphenylglycine 

Relevant articles and documents

Asymmetric synthesis of 1,2-diaryl-2-amino ethanols

A straightforward procedure for the asymmetric synthesis of 1,2-diaryl-2-amino ethanols is described. The key step relies on the diastereoselective electrophilic amination of the enolates derived from the corresponding (S,S)-(+)-pseudoephedrine arylacetam

Asymmetric synthesis of arylglycine amino acids using (S,S)-(+)- pseudoephedrine derived amides

Arylglycine aminoacids were obtained in good yields and with enantiomeric excesses higher than 99% by using an asymmetric amination reaction protocol on (S,S)-(+)-pseudoephedrine based arylacetamide enolates with di-tert-butylazodicarboxylate. Subsequent hydrazinolysis and hydrolysis yielded the target aminoacids.