185426-03-3

Basic information

• Product Name: (1S,2R,1'R)-(-)-N-<1-methyl-2-(2'-methyl-1'-nitromethylpropoxy)-2-phenylethyl>formamide
• Synonyms: (1S,2R,1'R)-(-)-N-<1-methyl-2-(2'-methyl-1'-nitromethylpropoxy)-2-phenylethyl>formamide
• CAS NO: 185426-03-3
• Molecular Weight: 294.351
• Mol File: 185426-03-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1S,2R,1'R)-(-)-N-<1-methyl-2-(2'-methyl-1'-nitromethylpropoxy)-2-phenylethyl>formamide(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R,1'R)-(-)-N-<1-methyl-2-(2'-methyl-1'-nitromethylpropoxy)-2-phenylethyl>formamide(185426-03-3)
• EPA Substance Registry System: (1S,2R,1'R)-(-)-N-<1-methyl-2-(2'-methyl-1'-nitromethylpropoxy)-2-phenylethyl>formamide(185426-03-3)

Safety Data

• Hazardous Substances Data: 185426-03-3(Hazardous Substances Data)

Upstream product

• 27675-38-3 (E)-3-methyl-1-nitro-but-1-ene 
• 77387-33-8 (1R,2S)-(-)-N-formylnorephedrine 
• 141377-55-1 3-methyl-1-nitrobutan-2-ol 

Downstream Products

• 185426-08-8 (1S,2R,1'R)-(-)-N-<2-(1'-tert-butoxycarbonylaminomethyl-2'-methylpropoxy)-1-methyl-2-phenylethyl>formamide 
• 185426-14-6 (2R)-(-)-1-tert-butoxycarbonylamino-3-methylbutan-2-ol 

Relevant articles and documents

Diastereo- and enantioselective synthesis of N-protected 2-amino 1,4-diols by an oxa Michael addition/1,3-dipolar cycloaddition protocol

An enantioselective synthesis of N-protected amino diols has been accomplished by employing a diastereoselective inter-and intramolecular 1,3-dipolar cycloaddition reaction of optically active nitrile oxides as a key step. The nitro alkane starting materi

Enantioselektive Synthese von vicinalen Aminoalkoholen durch Oxa-Michael-Addition

Keywords: Aminoalkohole; Asymmetrische Synthesen; Michael-Additionen; Nitroalkene; Synthesemethoden