109057-45-6

Basic information

• Product Name: Silane, trimethyl[1-(phenylseleno)-2-propenyl]-
• CAS NO: 109057-45-6
• Molecular Formula: C12H18SeSi
• Molecular Weight: 269.32
• Mol File: 109057-45-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Silane, trimethyl[1-(phenylseleno)-2-propenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, trimethyl[1-(phenylseleno)-2-propenyl]-(109057-45-6)
• EPA Substance Registry System: Silane, trimethyl[1-(phenylseleno)-2-propenyl]-(109057-45-6)

Safety Data

• Hazardous Substances Data: 109057-45-6(Hazardous Substances Data)

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 14370-82-2 allyl phenyl selenide 

Downstream Products

• 116142-48-4 Trimethyl-((E)-3-phenylselanyl-propenyl)-silane 
• 109057-52-5 heptaneselenoic acid Se-phenyl ester 
• 116142-47-3 (E)-1-Phenylselanyl-dec-1-en-4-one 
• 109057-62-7 Se-phenyl butaneselenoate 
• 116142-46-2 (E)-1-Phenylselanyl-non-1-en-4-one 
• 109057-51-4 Se-phenyl hexaneselenoate 
• 109057-50-3 Pentaneselenoic acid Se-phenyl ester 
• 116142-45-1 (E)-1-Phenylselanyl-oct-1-en-4-one 

Relevant articles and documents

A regioselective Aluminium Chloride-catalyzed Acylation of Allylic Selenides via α-Silyl Intermediates

The aluminium chloride-catalyzed acylation of α-silylallylic selenides with acid chlorides at -78 deg C produced γ-acylated vinylic selenides regioselectively. α-Silylallylic selenides in some cases underwent shifts of the selenenyl groups by the catalysis with aluminium chloride, affording γ-silylallylic selenides.This regioselective acylation of allylic selenides provides a new route to dihydrojasmone.