95712-47-3

Basic information

• Product Name: (1S*,4aR*,8aR*)-7-benzyl-1-methyl-4a,5,6,8a-tetrahydro-1H-pyrano<3,4-c>pyridin-8-(7H)-one
• CAS NO: 95712-47-3
• Molecular Weight: 257.332
• Mol File: 95712-47-3.mol

Chemical Properties

• CAS DataBase Reference: (1S*,4aR*,8aR*)-7-benzyl-1-methyl-4a,5,6,8a-tetrahydro-1H-pyrano<3,4-c>pyridin-8-(7H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (1S*,4aR*,8aR*)-7-benzyl-1-methyl-4a,5,6,8a-tetrahydro-1H-pyrano<3,4-c>pyridin-8-(7H)-one(95712-47-3)
• EPA Substance Registry System: (1S*,4aR*,8aR*)-7-benzyl-1-methyl-4a,5,6,8a-tetrahydro-1H-pyrano<3,4-c>pyridin-8-(7H)-one(95712-47-3)

Safety Data

• Hazardous Substances Data: 95712-47-3(Hazardous Substances Data)

Upstream product

• 95712-46-2 N-benzyl-N-crotonamide 
• 95712-41-7 1-methoxymethyloxypent-2(Z)-ene-5-ol 
• 95712-43-9 N-benzyl-N-(5-(methoxymethoxy)pent-3(Z)-enyl)amine 
• 95712-45-1 N-benzyl-N-<1-hydroxypent-2(Z)-en-5-yl>crotonamide 
• 95712-44-0 N-benzyl-N-<1-methoxymethyloxypent-2(Z)-en-5-yl>crotonamide 
• 108275-12-3 1-methoxymethyloxy-2-pentyn-5-ol 
• 95712-42-8 1-methoxymethyloxypent-2(Z)-enyl-5-p-toluenesulfonate 
• 95712-46-2 N-benzyl-N-crotonamide 

Downstream Products

• 108275-13-4 (1R*,3R*,4R*)-N-benzyl-3<1'(S*)-hydroxyethyl>-4-<2-(1'',3''-dithiano)ethyl>piperidine-2-one 
• 108275-14-5 (4R*)-N-benzyl-3(E)-ethylideno-4-<2-(1',3'-dithiano)ethyl>piperidine-2-one 
• 95712-49-5 methyl (1S*,4aS*,8aR*)-7-benzyl-4a,5,6,,7,8,8a-hexahydro-1-methyl-1H-pyrano<3,4-c>pyridine-4-carboxylate 
• 95712-48-4 (1S*,4aS*,8aR*)-7-benzyl-4a,5,6,,7,8,8a-hexahydro-1-methyl-1H-pyrano<3,4-c>pyridine 
• 108275-16-7 (1R*,3,4aS*,8aR*)-7-benzyl-3,4,4a,5,6,8a-hexahydro-3-methoxy-1-methyl-1H-pyrano<3,4-c>pyridin-8-(7H)-one 

Relevant articles and documents

APPLICATION OF THE INTRAMOLECULAR DIELS-ALDER REACTIONS OF HETERODIENES TO THE SYNTHESES OF INDOLE ALKALOIDS

A novel intramolecular Diels-Alder reaction involving the addition of an α,β-unsaturated aldehyde to an electron-deficient, dienophilic partner has been exploited as the key step in the development of a general entry to the heteroyohimboid and corynanthei