71443-23-7

Basic information

• Product Name: 2H-Pyran-3(6H)-one, 6-(phenylmethoxy)-
• CAS NO: 71443-23-7
• Molecular Formula: C12H12O3
• Molecular Weight: 204.225
• Mol File: 71443-23-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2H-Pyran-3(6H)-one, 6-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran-3(6H)-one, 6-(phenylmethoxy)-(71443-23-7)
• EPA Substance Registry System: 2H-Pyran-3(6H)-one, 6-(phenylmethoxy)-(71443-23-7)

Safety Data

• Hazardous Substances Data: 71443-23-7(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 35436-57-8 6-hydroxy-3,6-dihydro-2H-pyran-3-one 
• 19969-71-2 2,5-dimethoxy-2-hydroxymethyl-2,5-dihydrofuran 
• 98-00-0 (2-furyl)methyl alcohol 
• 62644-49-9 6-acetoxy-2H-pyran-3(6H)-one 
• 71443-22-6 1-O-benzoyl-2,3-dideoxy-D,L-pent-2-enopyranos-4-ulose 
• 100-44-7 benzyl chloride 

Downstream Products

• 126566-39-0 trans-4-Benzyloxy-5-hydroxy-2-cyclopenten-1-one 
• 122491-08-1 7-(Benzyloxy)-2-methylene-4-oxo-6-oxaperhydroindane 
• 122491-09-2 Spiro<<4(R^*)-(benzyloxy)-3-oxacyclohex-5-ene>-1,2'(S^*)-(4-methylenetetrahydrofuran)> 

Relevant articles and documents

Silica gel enables Achmatowicz rearrangement with KBr/oxone under “anhydrous” condition for one-pot functionalization

Silica gel was found to effectively promote Achmatowicz rearrangement (AchR) using KBr/oxone under near anhydrous condition. This new protocol allows direct functionalization of AchR products in a one-pot manner, effectively reducing the cost, time, and e

De novo asymmetric bio- and chemocatalytic synthesis of saccharides - Stereoselective formal O-glycoside bond formation using palladium catalysis

A novel integrated bio- and chemocatalytic approach to the de novo catalytic asymmetric synthesis of saccharides has been developed. Acetoxypyranones obtained enantiopure by enzymatic resolution have been shown to undergo highly stereoselective palladium-catalyzed formal O-glycoside bond formation. The combination of these protocols can be applied to the iterative asymmetric catalytic synthesis of saccharides. Copyright

Montmorillonite K-10 clay catalysed glycosidation of 1-O-acetyl-2,3-dideoxy-DL-pent-2-enopyrano-4-ulose

The O-glycosidation reaction of 1-O-acetyl-2,3-dideoxy-DL-pent-2-enopyran-4-ulose catalysed by the environmentally accepted and inexpensive industrial catalyst Montmorillonite K-10 clay with variety of alcohols in high yield is reported.