153941-58-3

Upstream product

• 153941-49-2 C₁₆H₁₂Cl₃NO₂S 

Downstream Products

• 1243630-41-2 C₂₀H₂₀N₂O₃S₂ 
• 1243630-45-6 4-tosyl-2-phenyl-5-p-chlorophenylsulphonyl-1,3-thiazole 
• 1243630-48-9 C₂₂H₁₇NO₂S₃ 
• 1243630-49-0 C₁₇H₁₅NO₂S₃ 
• 1243630-51-4 C₁₉H₁₇ClN₂O₃S₂ 
• 1243630-53-6 C₂₂H₁₇ClN₂O₂S₂ 
• 1243630-54-7 C₂₁H₁₄ClNO₃S₂ 
• 1243630-56-9 C₂₂H₁₆ClNO₃S₂ 
• 138537-80-1 C₁₆H₁₃NO₂S₃ 
• 1243630-38-7 C₂₃H₁₉NO₂S₃ 
• 1243630-44-5 C₂₃H₁₉NO₃S₂ 
• 1243630-43-4 C₂₂H₁₇NO₃S₂ 
• 1243630-40-1 C₂₂H₁₆ClNO₂S₃ 
• 1243630-42-3 C₂₃H₂₀N₂O₂S₂ 

Relevant academic research and scientific papers

Reactions of 4-tosyl-2-phenyl-5-chloro-1,3-thiazole with N-, O-, and S-nucleophiles

The accessible two-center electrophilic substrate 4-tosyl-2-phenyl-5- chloro-1,3-thiazole reacts regioselectively with N-, O-, and S-nucleophiles to eliminate a chloride ion. The analog of this substrate, 4-tosyl-2-phenyl-5-p- chlorophenylsulphonyl-1,3-th

Reaction of 1-tosyl-2,2-dichloroenamines with the Lawesson's reagent

In the reaction of the available 1-tosyl-2,2-dihlorenamides with the Lawesson's reagent the derivatives of 4-tosyl-1,3-thiazole were shown to form containing a labile chlorine atom at the C5 position. This fact was used for the synthesis of a number of the previously unknown bifunctionally substituted 4,5-thiazoles.