595566-39-5

Basic information

• Product Name: (3aR,6S,7R,7aS)-1-Benzyl-6-hydroxymethyl-6-methyl-hexahydro-pyrano[4,3-c]isoxazol-7-ol
• Synonyms: (3aR,6S,7R,7aS)-1-Benzyl-6-hydroxymethyl-6-methyl-hexahydro-pyrano[4,3-c]isoxazol-7-ol
• CAS NO: 595566-39-5
• Molecular Weight: 279.336
• Mol File: 595566-39-5.mol

Chemical Properties

• CAS DataBase Reference: (3aR,6S,7R,7aS)-1-Benzyl-6-hydroxymethyl-6-methyl-hexahydro-pyrano[4,3-c]isoxazol-7-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3aR,6S,7R,7aS)-1-Benzyl-6-hydroxymethyl-6-methyl-hexahydro-pyrano[4,3-c]isoxazol-7-ol(595566-39-5)
• EPA Substance Registry System: (3aR,6S,7R,7aS)-1-Benzyl-6-hydroxymethyl-6-methyl-hexahydro-pyrano[4,3-c]isoxazol-7-ol(595566-39-5)

Safety Data

• Hazardous Substances Data: 595566-39-5(Hazardous Substances Data)

Upstream product

• 595566-37-3 (3aR,5aS,6R,8aR,8bS)-1-Benzyl-5a-methyl-octahydro-2,5,8-trioxa-1-aza-as-indacene-6,7-diol 
• 595566-38-4 (3aR,6R,7R,7aS)-1-Benzyl-7-hydroxy-6-methyl-hexahydro-pyrano[4,3-c]isoxazole-6-carbaldehyde 
• 35784-67-9 (3aR,5R,6R,6aR)-5-[(4R)-2,2-dimethyl[1,3]dioxolan-4-yl]-2,2,6-trimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 174019-53-5 3-O-allyl-1,2:5,6-di-O-isopropylidene-3-C-methyl-α-D-allofuranose 
• 156742-39-1 3-O-allyl-1,2-O-isopropylidene-3-C-methyl-α-D-allofuranose 
• 170639-35-7 (3aR,5aR,6R,7R,8aR,8bS)-1-benzyl-5a-methyl-1,3,3a,5a,6,7,8a,8b-octahydro-6,7-isopropylideneoxy-4H-furo[2',3':3,2]pyrano[4,5-c]isoxazole 
• 156742-38-0 3-O-allyl-5-deoxy-1,2-O-isopropylidene-3-C-methyl-α-D-riboaldofuranose 
• 622-30-0 N-benzyl hydroxylalmine 

Relevant articles and documents

Synthesis of chiral oxepanes and pyrans by 3-O-allylcarbohydrate nitrone cycloaddition (3-OACNC)

3-O-Allylcarbohydrate nitrone cycloaddition (3-OACNC) furnished pyran and oxepane derivatives from 3-O-allyl hexose N-benzyl nitrones and 3-O-allyl furanoside-5-aldehyde N-benzyl/methyl nitrones. The regioselectivity of 3-OACNC was found to depend on the

Synthesis of enantiomeric pyrans from a 3-O-allylallose derivative by the application of intramolecular nitrone cycloaddition

The intramolecular nitrone cycloaddition of three sets of 3-O-allylpyranose and the corresponding homochiral 3-O-allylfuranose-5-aldehyde derivatives was studied; one set derived from D-allose gave rise to only pyran derivatives which were converted to en