54888-31-2

Upstream product

• 58956-86-8 p-chlorobenzoic acid N-1,2,2-trichloromethylamide 
• 56737-17-8 N-(2,2,2-trichloro-1-hydroxyethyl)-4-chlorobenzamide 
• 619-56-7 4-chlorobenzamide 
• 58956-81-3 N-(2,2-dichloro-1-hydroxyethyl)-4-chlorobenzamide 
• 53998-66-6 p-chlorobenzoic acid 1,2,2,2-tetrachloroethylamide 
• 64528-24-1 Methyl-N-(2.2-dichlorvinyl)p-chlorbenzimidat 

Downstream Products

• 64516-54-7 N-(2,2-dichlorovinyl)-4-chlorobenzimidoyl chloride 
• 90283-57-1 N-(1-Amino-2,2-dichloro-ethyl)-4-chloro-benzamide 
• 64563-89-9 4-chloro-N-(2,2-dichloro-vinyl)-thiobenzamide 
• 64528-24-1 Methyl-N-(2.2-dichlorvinyl)p-chlorbenzimidat 
• 64528-25-2 C₁₁H₁₁Cl₃N₂ 
• 64528-34-3 Methyl-N-(1-methoxy-2.2-dichlorethyl)-p-chlorbenzimidat 
• 64563-90-2 Methyl-N-(1.2.2.2-tetrachlorethyl)-p-chlorbenzimidat 
• 64528-39-8 N¹,N¹-Dimethyl-N²-(1.2.2.2-tetrachlorethyl)-p-chlor-benzamidin 
• 64528-46-7 N¹,N¹-Dimethyl-N²-(1-diethoxyphosphinyl-2.2.2-trichlorethyl)-p-chlorbenzamidin 
• 64528-28-5 4-[4-chloro-N-(2,2-dichloro-vinyl)-benzimidoyl]-morpholine 
• 64528-36-5 4-chloro-N-(2,2-dichloro-1-morpholin-4-yl-ethyl)-thiobenzamide 
• 1382676-05-2 N-(1-benzylsulfanyl-2,2-dichloroethyl)-4-chlorobenzamide 
• 1305711-66-3 2-(4-chlorophenyl)-1,3-thiazole-4-sulfonyl chloride 
• 1382676-35-8 4-benzylsulfanyl-2-(4-chlorophenyl)-1,3-thiazole 

Relevant academic research and scientific papers

Synthesis of Novel 3-Aryl-5-dichloromethyl-Δ2-1,2,4-oxadiazolines

The first synthetic approach to hitherto unknown 3-aryl-5-dichloromethyl-Δ2-1,2,4-oxadiazolines, of synthetic and biological interest, has been developed involving high-yield reactions between N-(2,2-dichlorovinyl)benzimidoyl chlorides and hydr

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.

Preparative conversion of chloralamides to 2,5-diaryl-3a,6a-dihydro-[1,3] thiazolo[4,5-d ]-[1,3]thiazoles with the Lawesson reagent

Based on readily available chloralamides, a preparative method for the synthesis of hitherto unknown 2,5-diaryl-3a,6a-dihydro[1,3]-thiazolo[4,5-d][1,3] thiazoles with the Lawesson reagent has been elaborated.

Sml2-mediated facile syntheses of N(2,2-dichlorovinyl)amides from acetates of chloralamide

Samarium diiodide-mediated elimination reaction provides a simple and general method to synthesise N-(2, 2-dichlorovinyl)amides 4 from acetates of chloralamides 3 in excellent yields. This novel reaction proceeds readily within a few minutes at room tempe

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