106130-40-9

Basic information

• Product Name: Thiazole, 4-phenyl-2-[(trichloromethyl)thio]-
• CAS NO: 106130-40-9
• Molecular Formula: C10H6Cl3NS2
• Molecular Weight: 310.655
• Mol File: 106130-40-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Thiazole, 4-phenyl-2-[(trichloromethyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Thiazole, 4-phenyl-2-[(trichloromethyl)thio]-(106130-40-9)
• EPA Substance Registry System: Thiazole, 4-phenyl-2-[(trichloromethyl)thio]-(106130-40-9)

Safety Data

• Hazardous Substances Data: 106130-40-9(Hazardous Substances Data)

Upstream product

• 70-11-1 α-bromoacetophenone 
• 104942-40-7 O-ethyl-S-(2-oximino-2-phenylethyl)dithiocarbonate 
• 104942-45-2 4-phenyl-3-hydroxythiazole-2(3H)-thione 
• 14181-72-7 2-bromo-1-phenyl-ethanone oxime 
• 106130-34-1 3-palmitoyloxy-4-phenylthiazolin-2(3H)-thione 
• 75-62-7 Bromotrichloromethane 

Relevant articles and documents

The Invention of New Radical Chain Reactions. Part 9. Further Radical Chemistry of Thiohydroxamic Esters; Formation of Carbon-Carbon Bonds

Carbon radicals derived from the esters of several types of thiohydroxamic acids have been trapped in a number of different ways.Particular attention has been paid to carbon-carbon bond formation by addition to suitably activated ethylenic linkages.Carboxylic acids can be conveniently converted into homo- and bishomo-acids by free radical chemistry based on thiohydroxamic esters.In a coda the tautomerism of the thiohydroxamic acids have been examined by physical methods.It is confirmed that the esters used are derivatives of the thione tautomer.