80399-01-5

Basic information

• Product Name: Trimethyl-((1E,4E)-4-phenylsulfanyl-hepta-1,4-dienyloxy)-silane
• CAS NO: 80399-01-5
• Molecular Weight: 292.517
• Mol File: 80399-01-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Trimethyl-((1E,4E)-4-phenylsulfanyl-hepta-1,4-dienyloxy)-silane(CAS DataBase Reference)
• NIST Chemistry Reference: Trimethyl-((1E,4E)-4-phenylsulfanyl-hepta-1,4-dienyloxy)-silane(80399-01-5)
• EPA Substance Registry System: Trimethyl-((1E,4E)-4-phenylsulfanyl-hepta-1,4-dienyloxy)-silane(80399-01-5)

Safety Data

• Hazardous Substances Data: 80399-01-5(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 80398-85-2 1-Phenylsulfanyl-3-oxa-bicyclo[3.1.0]hexan-2-ol 
• 80398-84-1 (E)-2-(hydroxymethyl)cyclopropyl phenyl sulphide 
• 63196-76-9 Methyl trans-2-phenylthiocyclopropanecarboxylate 
• 29193-71-3 methyl 4-(phenylsulfanyl)butanoate 
• 80398-89-6 Trimethyl-[2-phenylsulfanyl-2-((Z)-propenyl)-cyclopropylmethoxy]-silane 
• 80398-84-1 (2-Phenylsulfanyl-cyclopropyl)-methanol 
• 80398-85-2 (1S,5R)-1-Phenylsulfanyl-3-oxa-bicyclo[3.1.0]hexan-2-ol 
• 80398-89-6 Trimethyl-[(1S,2S)-2-phenylsulfanyl-2-((E)-propenyl)-cyclopropylmethoxy]-silane 

Downstream Products

• 18492-65-4 7,7-diethoxy-hept-3c-ene 
• 80575-02-6 [(E)-1-(3,3-Dimethoxy-propyl)-but-1-enylsulfanyl]-benzene 
• 80575-01-5 [(E)-1-(3,3-Diethoxy-propyl)-but-1-enylsulfanyl]-benzene 

Relevant articles and documents

STRAIN AND SELECTIVITY: PARTNERS FOR ORGANIC SYNTHESIS

The development of two new small-ring conjunctive reagents, (E)-2-(hydrohymethyl)cyclopropyl phenyl sulphide and 1,1-bis(benzenesulphonyl)cyclopropane, are reported.The former permits a synthesis of 2,4-disubstituted cyclobutanones and (E)-4-phenylthio-4-

A CHEMOSELECTIVE DESULFURIZATION METHOD VIA HOMOGENEOUS NICKEL CATALYSIS

Isopropylmagnesium bromide in the presence of bis-(triphenylphosphino)-nickel(II) chloride reduces vinyl sulfides stereospecifically to the corresponding olefins without overreduction - a process which serves as a key step in the synthesis of the sex pheromone of the Douglas fir tussock moth.