33331-97-4

Basic information

• Product Name: 4-methyl-3,4-epoxytetrahydropyran
• CAS NO: 33331-97-4
• Molecular Weight: 114.144
• Mol File: 33331-97-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-methyl-3,4-epoxytetrahydropyran(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-3,4-epoxytetrahydropyran(33331-97-4)
• EPA Substance Registry System: 4-methyl-3,4-epoxytetrahydropyran(33331-97-4)

Safety Data

• Hazardous Substances Data: 33331-97-4(Hazardous Substances Data)

Upstream product

• 16302-35-5 4-methyl-3,6-dihydro-2H-pyran 

Downstream Products

• 129673-36-5 ((3R,4R)-4-Hydroxy-4-methyl-tetrahydro-pyran-3-ylamino)-acetic acid 
• 134259-24-8 3-((3R,4R)-4-Hydroxy-4-methyl-tetrahydro-pyran-3-ylamino)-propionic acid 
• 133478-30-5 4-hydroxy-4-methyl-3-tetrahydropyranylcyclohexylsulfone 
• 133478-29-2 4-hydroxy-4-methyl-3-tetrahydropyranyl-cyclohexylsulfoxide 
• 84186-22-1 4-methyl-3-piperidinotetrahydropyran-4-ol p-nitrobenzoate 
• 90072-80-3 (3-Methyl-tetrahydro-furan-3-yl)-phenyl-methanol 
• 133478-22-5 4-hydroxy-4-methyl-3-phenoxytetrahydropyran 
• 134259-25-9 4-((3R,4R)-4-Hydroxy-4-methyl-tetrahydro-pyran-3-ylamino)-butyric acid 
• 129673-47-8 2-Benzoylamino-3-methyl-butyric acid (3S,4S)-4-hydroxy-4-methyl-tetrahydro-pyran-3-yl ester 
• 133478-32-7 4-hydroxy-4-methyltetrahydropyran-3-yl benzoate 
• 133478-36-1 S-(4-hydroxy-4-methyltetrahydropyran-3-yl)thiouronium sulfate 
• 16302-35-5 4-methyl-3,6-dihydro-2H-pyran 
• 129673-46-7 3-Phenyl-2-(toluene-4-sulfonylamino)-propionic acid (3R,4R)-4-hydroxy-4-methyl-tetrahydro-pyran-3-yl ester 
• 129673-48-9 2-Acetylamino-3-phenyl-propionic acid (3S,4S)-4-hydroxy-4-methyl-tetrahydro-pyran-3-yl ester 

Relevant articles and documents

Substituted alkenediols by alkylative double ring opening of dihydrofuran and dihydropyran epoxides

Equation presented Dihydrofuran and dihydropyran epoxides undergo alkylative double ring opening with organolithiums to provide a new route to substituted alkenediols.

Reaction of tetrahydropyranyl azides with 5-R-bicyclo[2.2.1]-2-heptenes

The reaction of 5-R-bicyclo[2.2.1]-2-heptenes with 3-azido-4-hydroxy-4-methyltetrahydropyran and 4-azidomethyl-4-hydroxytetrahydropyran, obtained by opening the oxirane ring in epoxytetrahydropyrans with sodium azide, leads to the formation of N-tetrahydropyranylaziridines with 100% stereoselectivity. 1998 Plenum Publishing Corporation.