63499-60-5

Upstream product

• 302-17-0 chloral hydrate 
• 619-55-6 para-methylbenzamide 
• 75-87-6 chloral 

Downstream Products

• 63499-51-4 3-(4-methyl-benzoyl)-2-trichloromethyl-oxazolidine-4,5-dione 
• 61767-28-0 N-(1,2,2,2-tetrachloroethyl)-4-methylbenzamide 
• 61767-26-8 N-(2,2-dichloro-1-cyanovinyl)-4-methylbenzamide 
• 898507-91-0 N-(1-benzylsulfanyl-2,2-dichloroethyl)-4-methylbenzamide 
• 1000613-41-1 4-benzylsulfanyl-2-(4-methylphenyl)-1,3-thiazole 
• 1382676-58-5 2-(4-methylphenyl)-1,3-thiazole-4-sulfonyl chloride 
• 86521-52-0 <1-(4-methylbenzoylamino)-2,2-dichlorovinyl>triphenylphosphonium chloride 
• 54682-94-9 N-(1,2,2,2-tetrachloroethyl)-4-methylbenzimidoyl chloride 
• 54888-30-1 N-(2,2-dichlorovinyl)-4-methylbenzamide 

Relevant academic research and scientific papers

A new, high-yield synthesis of 3-aryl-1,2,4-triazoles

A convenient new synthetic approach to 3-aryl-1,2,4-triazoles has been developed. Chloralamides were obtained by high yield reactions between benzamides and chloral hydrate. These reacted with a phosphorus pentachloride/phosphorus oxychloride mixture unde

A facile synthesis of 1,3-thiazole-4-sulfonyl chlorides

(Chemical Equation Presented) A four-step preparative-scale synthesis of eight 2-alkyl- and arylsubstituted thiazole-4-sulfonyl chlorides from chloralamides is reported. Good yields and easy availability of starting materials are valuable advantages of the procedure that gives access to formerly unattainable building blocks. Copyright Taylor & Francis Group, LLC.

Potassium channel openers

Compounds of formula I: are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.

Potassium channel openers

Compounds of formula I: are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.

Electrochemical generation of N-(2,2-dichlorovinyl)amides

A convenient method for the synthesis of N-(2,2-dichlorovinyl)amides has been established. Treatment of chloralamides with phosphorus pentachloride provides N-(1,2,2,2-tetrachloroethyl)amides in high yields whose electrochemical reduction leads to the tit