448896-88-6

Basic information

• Product Name: 3H-Oxazolo[3,4-a]pyridin-3-one, 1,5,8,8a-tetrahydro-8-hydroxy-, (8R,8aS)- (9CI)
• Synonyms: 3H-Oxazolo[3,4-a]pyridin-3-one, 1,5,8,8a-tetrahydro-8-hydroxy-, (8R,8aS)- (9CI)
• CAS NO: 448896-88-6
• Molecular Formula: C₇H₉NO₃
• Molecular Weight: 155.15126
• Product Categories: ALCOHOL
• Mol File: 448896-88-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3H-Oxazolo[3,4-a]pyridin-3-one, 1,5,8,8a-tetrahydro-8-hydroxy-, (8R,8aS)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Oxazolo[3,4-a]pyridin-3-one, 1,5,8,8a-tetrahydro-8-hydroxy-, (8R,8aS)- (9CI)(448896-88-6)
• EPA Substance Registry System: 3H-Oxazolo[3,4-a]pyridin-3-one, 1,5,8,8a-tetrahydro-8-hydroxy-, (8R,8aS)- (9CI)(448896-88-6)

Safety Data

• Hazardous Substances Data: 448896-88-6(Hazardous Substances Data)

Upstream product

• 25791-21-3 3-benzyloxycarbonylamino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allo-1,4-furanose 
• 1346679-04-6 C₁₄H₁₇NO₄ 
• 1346679-03-5 3-[(allyl)(benzyloxycarbonyl)amino]-3-deoxy-1,2-O-isopropylidene-α-D-allo-1,4-furanose 
• 1346679-02-4 3-[(allyl)(benzyloxycarbonyl)amino]-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allo-1,4-furanose 
• 910479-41-3 Allyl-((3aR,5R,6R,6aR)-2,2-dimethyl-5-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-carbamic acid benzyl ester 
• 837375-05-0 (S)-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]oxazolidin-2-one 
• 1278522-14-7 (8R,8aS)-8-(t-butyldimethylsilyloxy)-8,8a-dihydro-1H-oxazolo[3,4-a]pyridin-3(5H)-one 
• 1278522-12-5 (S)-3-allyl-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]oxazolidin-2-one 
• 1278522-07-8 (2S,3R,E)-3-(t-butyldimethylsilyloxy)-2-[(R)-1-phenylethylamino]hex-4-en-1-ol 
• 1278522-05-6 (2S,3R,E)-3-(t-butyldimethylsilyloxy)-2-[(R)-1-phenylethylamino]hex-4-enyl acetate 
• 1278522-03-4 (S)-2-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]-1-[(R)-1-phenylethyl]aziridine 
• 1278522-01-2 (R,E)-1-{(S)-1-[(R)-1-phenylethyl]aziridin-2-yl}but-2-en-1-ol 
• 1278521-99-5 (R)-1-{(S)-1-[(R)-1-phenylethyl]aziridin-2-yl}but-2-yn-1-ol 
• 1278521-97-3 1-{(S)-1-[(R)-1-phenylethyl]aziridin-2-yl}but-2-yn-1-one 

Downstream Products

• 849928-62-7 (8R,8aS)-8-hydroxyhexahydrooxazolo[3,4-a]pyridin-3-one 
• 849928-63-8 (8R,8aS)-8-benzyloxyhexahydrooxazolo[3,4-a]pyridin-3-one 
• 849928-65-0 (2R,3R)-3-Benzyloxy-2-formyl-piperidine-1-carboxylic acid tert-butyl ester 
• 849928-71-8 (1S,2R,8R,8aS)-8-benzyloxy-1,2-dihydroxyhexahydroindolizin-3-one 
• 849928-64-9 tert-butyl (2S,3R)-3-(benzyloxy)-2-(hydroxymethyl)piperidine-1-carboxylate 
• 849928-69-4 (2S,3R,1'S,2'R)-N-tert-butoxycarbonyl-3-benzyloxy-2-[2'-ethoxycarbonyl-1',2'-dihydroxyethyl]piperidine 

Relevant articles and documents

Chiron approach strategy to the bicyclic oxazolidinylpiperidine: A building block for preparing mono-and bi-cyclic iminosugars

A chiron approach to the synthesis of bicyclic oxazolidinylpiperidine, a synthetically potential building block for preparing mono-and bi-cyclic iminosugars, is reported from D-glucose using ring closing metathesis as the key step.

General approach to glycosidase inhibitors. Enantioselective synthesis of deoxymannojirimycin and swainsonine

(Chemical Equation Presented) Deoxymannojirimycin (2) and swainsonine (4) have been synthesized from each enantiomer of the same bicyclic carbarnate precursor 7. The key intermediate was prepared by a simple and efficient three-step synthesis involving RCM of the diene 8, which in turn is easily accessible in any configuration from enantiomerically enriched 2,3-epoxy-4-penten-1-ol 9.