29431-43-4

Upstream product

• 58956-84-6 benzoic acid N-1,2,2-trichloromethylamide 
• 55-21-0 benzamide 
• 75-87-6 chloral 
• 58956-88-0 N-Benzoyl-1-(p-chlorphenylthio)-2,2-dichloraethylamin 
• 6780-37-6 N-(2,2,2-Trichloroethylidene)benzamide 
• 6316-07-0 N-(2,2,2-trichloro-1-hydroxyethyl)benzamide 
• 6798-35-2 N-(1,2,2,2-tetrachloroethyl)benzamide 
• 58956-79-9 N-(2,2-dichloro-1-hydroxy-ethyl)-benzamide 
• 6780-31-0 2-acetoxy-2-benzoylamino-1,1,1-trichloro-ethane 

Downstream Products

• 51945-75-6 N-(2-bromo-2,2-dichloro-1-hydroxy-ethyl)-benzamide 
• 58956-79-9 N-(2,2-dichloro-1-hydroxy-ethyl)-benzamide 
• 58956-84-6 benzoic acid N-1,2,2-trichloromethylamide 
• 34509-03-0 N-(2,2-dichloro-1-ethoxyethyl)benzamide 
• 61833-99-6 N-(2,2-dichlorovinyl)benzimidoyl chloride 
• 59776-42-0 N-(2,2-dichloro-1-diethylaminoethyl)benzamide 
• 79054-59-4 1,1,1-trichloro-2-benzenesulfonamido-2-benzamidoethane 
• 131941-85-0 N,N-bis(2,2,2-trichloro-1-benzamidoethyl)benzenesulfonamide 
• 76543-32-3 N¹,N¹-dimethyl-N²-(2,2-dichloro-1-benzoylaminoethyl)benzamidine 
• 132281-41-5 1,1,1-trichloro-2-p-chlorobenzenesulfonamido-2-benzamidoethane 
• 76543-31-2 N-(1-benzoylamino-2,2-dichloroethyl)benzamidine 
• 90283-55-9 N-(1-amino-2,2-dichloroethyl)benzamide 
• 130775-21-2 N-(2,2-Dichloro-1-p-tolylsulfanyl-ethyl)-benzamide 
• 130775-25-6 N-(2,2-Dichloro-1-p-tolylsulfanyl-ethyl)-thiobenzamide 

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

A new synthetic route to 2-oxazolines. The electrochemical reduction of N-(2,2-dichloroethyl)amides as a key step

A convenient new method for the synthesis of 2-oxazolines has been established involving the preparation of N-(2,2-dichloroethyl)amides followed by electrochemical reductive cyclizations. It has been applied successfully in preparing previously unknown 4-

SYNTHESIS OF FUNCTIONALLY 4-SUBSTITUTED OXAZOLES AND THIAZOLES BASED ON N-(2,2-DICHLOROETHENYL)AMIDES OF CARBOXYLIC AND THIOCARBOXYLIC ACIDS

Successive treatment of enamides Cl2C=CHNHC(O)R first with ammonia and then with carboxylic acid chlorides and sodium methoxide gave a series of previously unkown 2-substituted 4-acylaminooxazoles.The enamides of thiocarboxylic acids Cl2C=CHNHC(S)R react