1241959-25-0

Basic information

• Product Name: (R,E)-N-((S)-1-(benzyloxy)but-3-en-2-yl)-2-(tert-butyldiphenylsilyloxy)pent-3-en-1-amine
• Synonyms: (R,E)-N-((S)-1-(benzyloxy)but-3-en-2-yl)-2-(tert-butyldiphenylsilyloxy)pent-3-en-1-amine
• CAS NO: 1241959-25-0
• Molecular Weight: 499.769
• Mol File: 1241959-25-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R,E)-N-((S)-1-(benzyloxy)but-3-en-2-yl)-2-(tert-butyldiphenylsilyloxy)pent-3-en-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (R,E)-N-((S)-1-(benzyloxy)but-3-en-2-yl)-2-(tert-butyldiphenylsilyloxy)pent-3-en-1-amine(1241959-25-0)
• EPA Substance Registry System: (R,E)-N-((S)-1-(benzyloxy)but-3-en-2-yl)-2-(tert-butyldiphenylsilyloxy)pent-3-en-1-amine(1241959-25-0)

Safety Data

• Hazardous Substances Data: 1241959-25-0(Hazardous Substances Data)

Upstream product

• 97682-96-7 (2S)-1-(phenylmethoxy)but-3-en-2-ylamine 
• 6812-26-6 (R)-(-)-2-hydroxy-3-(E)-pentenenitrile 

Downstream Products

• 1241959-28-3 tert-butyl (S)-1-(benzyloxy)but-3-en-2-yl((R,E)-2-(tert-butyldiphenylsilyloxy)pent-3-enyl)carbamate 
• 1241959-29-4 tert-butyl (3R,6S)-6-((benzyloxy)methyl)-3-((tert-butyldiphenylsilyl)oxy)-3,6-dihydropyridine-1(2H)-carboxylate 
• 1241959-33-0 (2R,3R,4S,5S)-tert-butyl 2-((benzyloxy)methyl)-5-(tert-butyldiphenylsilyloxy)-3,4-dihydroxypiperidine-1-carboxylate 
• 1241959-34-1 (2R,3S,4R,5S)-tert-butyl 2-((benzyloxy)methyl)-5-(tert-butyldiphenylsilyloxy)-3,4-dihydroxypiperidine-1-carboxylate 
• 1393105-79-7 C₂₁H₃₁NO₆ 
• 1393105-81-1 C₂₁H₃₁NO₆ 
• 1393105-84-4 tert-butyl (2S,5S)-2-(benzyloxymethyl)-5,6-dihydro-5-hydroxypyridine-1(2H)-carboxylate 
• 1393106-05-2 C₃₇H₄₉NO₆Si 
• 1393106-07-4 C₂₁H₂₉NO₆ 
• 1393106-09-6 tert-butyl (2S,5R)-2-(benzyloxymethyl)-5,6-dihydro-5-hydroxypyridine-1(2H)-carboxylate 
• 1393106-11-0 tert-butyl (2S,5S)-5-benzoyloxy-2-(benzyloxymethyl)-5,6-dihydropyridine-1(2H)-carboxylate 
• 1393106-13-2 tert-butyl (2R,3R,4S,5R)-2-benzyloxymethyl-3,4,5-trihydroxypiperidine-1-carboxylate 

Relevant articles and documents

Synthesis of eight 1-deoxynojirimycin isomers from a single chiral cyanohydrin

Eight configurational 1-deoxynojirimycin isomers have been synthesized starting from a chiral cyanohydrin as the common precursor. The cyanohydrin chiral pool building block is easily accessible in large quantities by using almond hydroxynitrile lyase as the chiral catalyst in condensing hydrogen cyanide and crotonaldehyde. Our work complements the large body of literature on the synthesis of 1-deoxynojirimycin derivatives with the distinguishing feature that eight stereoisomers of this important class of glycosidase inhibitors can be derived from a common precursor in an efficient manner.