1217341-14-4

Basic information

• Product Name: C₁₈H₂₃NO₂
• Synonyms: C₁₈H₂₃NO₂
• CAS NO: 1217341-14-4
• Molecular Weight: 285.386
• Mol File: 1217341-14-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₈H₂₃NO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₂₃NO₂(1217341-14-4)
• EPA Substance Registry System: C₁₈H₂₃NO₂(1217341-14-4)

Safety Data

• Hazardous Substances Data: 1217341-14-4(Hazardous Substances Data)

Upstream product

• 51673-84-8 dimethoxyacetaldehyde 
• 100-46-9 benzylamine 
• 6921-34-2 benzylmagnesium chloride 
• 701954-53-2 benzyl[(2,2-dimethoxy)ethylidene]amine 

Downstream Products

• 1084820-36-9 (R)-1-benzyl-2,2-dimethoxyethylamine 
• 1184944-94-2 (R)-1-benzyl-2,2-dimethoxyethylammonium N-acetyl-L-phenylalaninate 
• 1184944-95-3 (S)-1-benzyl-2,2-dimethoxyethylammonium N-acetyl-D-phenylalaninate 
• 59830-60-3 N-benzyloxycarbonyl-2-amino-3-phenylpropionaldehyde 
• 6372-14-1 (2S)-2-(N-benzyloxycarbonyl)-amino-3-phenyl propanol 
• 59830-61-4 benzyl 1-benzyl-2,2-dimethoxyethylcarbamate 
• 55707-43-2 (S)-1-benzyl-2,2-dimethoxyethan-1-amine 
• 55707-43-2 1-benzyl-2,2-dimethoxyethylamine 

Relevant articles and documents

Resolution and absolute configuration of some a-aminoacetals: En route to enantiopure N-protected a-aminoaldehydes

The first successful resolution of rac-a-aminoacetals via diastereoisomeric salt formation with optically pure N-protected aminoacids is reported. The absolute configuration assignment of a-aminoacetal enantiomers is performed by an entirely non-racemizing chemical correlation method involving N-protection and a new efficient hydrolysis step followed by a reduction of the resulting N-protected a-aminoaldehyde intermediates. A racemization method of optically enriched a-aminoacetals is exemplified to allow valorisation of both enantiomers. Springer-Verlag 2011.