134022-41-6

Basic information

• Product Name: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-, trans-
• CAS NO: 134022-41-6
• Molecular Formula: C12H16OSe
• Molecular Weight: 255.218
• Mol File: 134022-41-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-, trans-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-, trans-(134022-41-6)
• EPA Substance Registry System: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-, trans-(134022-41-6)

Safety Data

• Hazardous Substances Data: 134022-41-6(Hazardous Substances Data)

Upstream product

• 5707-04-0 Phenylselenyl chloride 
• 928-92-7 (E)-hex-4-en-1-ol 
• 34837-55-3 Phenylselenyl bromide 
• 1666-13-3 diphenyl diselenide 

Relevant articles and documents

A mild and efficient procedure for alkenols oxyselenocyclization by using ionic liquids

A mild and efficient procedure for the oxyselenocyclization of unsaturated alcohols by treatment with phenylselenyl chloride using ionic liquids as solvents/catalyzers has been developed. The reaction proceeds instantaneously under mild conditions with ab

Regio- and stereoselectivity in phenylselenoetherification of (Z)- and (E)-hex-4-en-1-ols

Δ4-Primary alkenols (Z)- and (E)-hex-4-en-l-ols underwent facile cyclization to the corresponding phenyl selenoethers using PhSeX (X = Cl, Br) in high yields and in good to excellent selectivities in the presence of some catalysts (Lewis acids

Molecular orbital study of the rearrangement of seleniranium ions

The mechanism of phenylselenoetherification of unsaturated alcohols, involving seleniranium cationic intermediates, is studied by the semiempirical molecular-orbital MNDO-PM3 method.Results of calculation on several Δ4-alkenols attacked by PhSe