2533-68-8

Usage

Physical state

white solid

Solubility

soluble in water and other polar solvents

Also known as

N-chloroacetyl-N’-trichloroacetyldiazine

Common uses

reagent for the synthesis of various organic compounds, particularly in the pharmaceutical and agricultural industries, intermediate in the production of dyes and other industrial chemicals

Versatility

wide range of applications in chemical synthesis and various industrial processes

Upstream product

• 545-06-2 trichloroacetonitrile 
• 42563-95-1 2,2-dichloro-4-trichloromethyl-2λ⁵-[1,3,2]diazaphosphete 
• 2533-69-9 methyl 2,2,2-trichloroacetimidate 
• 22259-53-6 3-aminomethylindole 
• 71-43-2 benzene 
• 7664-41-7 ammonia 

Downstream Products

• 4122-04-7 2-amino-1,3,5-triazine 
• 20376-31-2 2-amino-4,6-bis(trichloromethyl)-1,3,5-triazine 
• 82805-41-2 2-Trifluoromethyl-2-phenyl-4,6-bis(trichloromethyl)-1,2-dihydro-sym-triazine 
• 143034-54-2 N,N-Dimethyl-N'-(2,2,2-trichloro-1-imino-ethyl)-benzamidine 
• 42563-97-3 trichloroacetamidine hydrochloride 
• 80862-23-3 2-trichloromethyl-4-trifluoromethyl-5-cyano-6-aminopyrimidine 
• 80862-24-4 2-trichloromethyl-4-trifluoromethyl-5-trifluoromethylthio-6-aminopyrimidine 
• 611-74-5 N,N-dimethylbenzamide 
• 16088-73-6 6-trichloromethyl-[1,3,5]triazine-2,4-diamine 
• 67-66-3 chloroform 
• 7664-41-7 ammonia 
• 90348-96-2 N-phenylthiocarbamoyltrichloroacetamidine 
• 930608-33-6 (Z)-5-phenylpent-2-enyl 2,2,2-trichloroacetimidate 

Relevant academic research and scientific papers

Oligomerization of Trichloroacetonitrile (TCA) by Metal Salts

A CN bond was found to transform into a C=N bond under such a mild conditions as to mix trichloroacetonitrile, metal salts and methanol at 20 deg C.Ni(II) and Co(II) gave dimeric ring complexes and Mn(II) gave amidine, aminotriazine and brown powder.The aminotriazine was isolated as unstable liquid which spontaneously transformed into the crystal.A trimer structure was proposed for the liquid.In anhydrous systems, any oligomerization did not occur, so water was concluded to participate in the initiation.Keywords - trichloroacetonitrile; metal salt; methanol; nitrile; imino bond; dimeric ring complex; amidine; aminotriazine; trimer

Process for the preparation of substituted trichloroacetamidine derivatives

Substituted trichloroacetamidine derivatives are prepared by treating an appropriately substituted imidate with ammonia. The imidate intermediates are prepared by treating an appropriately substituted amine with an imidating reagent.