65275-53-8

Basic information

• Product Name: Benzene, [(2-phenylethyl)seleninyl]-
• CAS NO: 65275-53-8
• Molecular Formula: C14H14OSe
• Molecular Weight: 277.225
• Mol File: 65275-53-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzene, [(2-phenylethyl)seleninyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(2-phenylethyl)seleninyl]-(65275-53-8)
• EPA Substance Registry System: Benzene, [(2-phenylethyl)seleninyl]-(65275-53-8)

Safety Data

• Hazardous Substances Data: 65275-53-8(Hazardous Substances Data)

Upstream product

• 65275-36-7 (2-phenyl-ethyl) phenyl selenide 

Downstream Products

• 1386397-44-9 C₁₆H₁₆O₂Se 
• 25570-56-3 (RS)-1-(phenylseleno)-2-propanol 
• 28897-11-2 2-methyl-1-(phenylselanyl)propan-2-ol 
• 51558-95-3 1-phenyl-2-(phenylselanyl)ethanol 
• 63603-28-1 1-methoxy-1-phenyl-2-phenylselenoethane 
• 63603-31-6 methyl 1-phenylselenenyl-2-octyl ether 
• 52954-45-7 β-hydroxyoctyl phenyl selenide 
• 60221-17-2 1-(phenylseleno)dodecan-2-ol 
• 100-42-5 styrene 
• 5818-99-5 benzeneselenenic acid 

Relevant articles and documents

Intermolecular radical reaction of O, Se-acetals generated via seleno-Pummerer rearrangement

A new general protocol for the synthesis of O,Se-acetals using the seleno-Pummerer reaction has been developed, and their radical-based two- and three-component coupling reactions were studied. The three-component coupling employed the O,Se-acetal, cyclopentenone, and an allylstannane derivative, and enabled stereoselective installations of α-acyloxy alkyl and functionalized allyl groups to generate the 2,3-trans-disubstituted cyclopentanone in a single operation. The obtained highly functionalized structure was used as an intermediate for facile assembly of the zedoarondiol carboskeleton.