857900-11-9

Basic information

• Product Name: N-{(1S)-1-[(methoxy)methyl]-2-methylpropyl}-N-{(1E)-phenyl[(2S)-2-phenyl-3,4-dihydropyridin-1(2H)-yl]methylene}amine
• Synonyms: N-{(1S)-1-[(methoxy)methyl]-2-methylpropyl}-N-{(1E)-phenyl[(2S)-2-phenyl-3,4-dihydropyridin-1(2H)-yl]methylene}amine
• CAS NO: 857900-11-9
• Molecular Weight: 362.515
• Mol File: 857900-11-9.mol

Chemical Properties

• CAS DataBase Reference: N-{(1S)-1-[(methoxy)methyl]-2-methylpropyl}-N-{(1E)-phenyl[(2S)-2-phenyl-3,4-dihydropyridin-1(2H)-yl]methylene}amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-{(1S)-1-[(methoxy)methyl]-2-methylpropyl}-N-{(1E)-phenyl[(2S)-2-phenyl-3,4-dihydropyridin-1(2H)-yl]methylene}amine(857900-11-9)
• EPA Substance Registry System: N-{(1S)-1-[(methoxy)methyl]-2-methylpropyl}-N-{(1E)-phenyl[(2S)-2-phenyl-3,4-dihydropyridin-1(2H)-yl]methylene}amine(857900-11-9)

Safety Data

• Hazardous Substances Data: 857900-11-9(Hazardous Substances Data)

Upstream product

• 386253-34-5 (S)-1-methoxy-3-methyl-N(phenyl((S)-2-phenylpyridin-1(2H)-yl)methylene)butan-2-amine 

Downstream Products

• 1071527-60-0 N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-N-[(1E)-phenyl-[(2S)-2-phenyl-5-(3-trifluoromethylphenyl)-3,4-dihydropyridin-1(2H)-yl](phenyl)methylene]amine 
• 911694-20-7 N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-N-[(1E)-[(2S)-5-(4-methoxyphenyl)-2-phenyl-3,4-dihydropyridin-1(2H)-yl](phenyl)methylidene]amine 
• 1071527-59-7 N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-N-[(1E)-[(2S)-5-(3-methylphenyl)-2-phenyl-3,4-dihydropyridin-1(2H)-yl](phenyl)methylene]amine 
• 911694-22-9 N-[(1E)-[(2S)-2,5-diphenyl-3,4-dihydropyridin-1(2H)-yl](phenyl)methylidene]-N-[(1S)-1-(methoxymethyl)-2-methylpropyl]amine 
• 911694-13-8 N-[(1E)-[(2S)-5-iodo-2-phenyl-3,4-dihydropyridin-1(2H)-yl](phenyl)methylidene]-N-[(1S)-1-(methoxymethyl)-2-methylpropyl]amine 

Relevant articles and documents

Stereoselective synthesis of 2,6-disubstituted 3-piperidinols: Application to the expedient synthesis of (+)-julifloridine

(Chemical Equation Presented) The asymmetric synthesis of 2,6-disubstituted 3-piperidinols having a 2,3-cis and 2,6-trans relative stereochemistry was accomplished in three steps using the following sequence: stereocontrolled nucleophilic addition of an o