4826-06-6

Upstream product

• 7035-69-0 N′-(4-chlorophenyl)benzamidine 
• 50839-53-7 7-chloro-1-morpholino-3-phenyl-1λ⁴,2,4-benzothiadiazine 
• 50839-52-6 1,7-dichloro-3-phenyl-1,2,4-benzothiadiazine 
• 4825-98-3 3-phenyl-1-(toluene-4-sulfonylamino)-1λ⁴-benzo[1,2,4]thiadiazine 
• 4826-01-1 1-methanesulfonylamino-3-phenyl-1λ⁴-benzo[1,2,4]thiadiazine 
• 7035-69-0 (Z)-N'-(4-chlorophenyl)benzimidamide 
• 4825-99-4 7-chloro-3-phenyl-1-(toluene-4-sulfonylamino)-1λ⁴-benzo[1,2,4]thiadiazine 
• 4826-05-5 1-oxo-3-phenyl-2H-1,2,4-benzothiadiazine 
• 89983-51-7 C₁₃H₁₀Cl₂N₂ 
• 1527-91-9 N-phenylbenzamidine 

Downstream Products

• 20043-39-4 7-chloro-3-phenyl-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide 
• 20043-30-5 7-chloro-3-phenyl-2H-1,2,4-benzothiadiazine 

Relevant academic research and scientific papers

REACTION OF N-CHLORO-N'-ARYLBENZAMIDINES WITH SULFUR DICHLORIDE. 1-CHLORO-3-R-1,2,4-BENZOTHIADIAZINES

1-Chloro-3-R-1,2,4-benzothiadiazines are produced in the reaction of N-chloro-N'-arylbenzamidines with sulfur dichloride in the presence of pyridine.During hydrolysis they are converted into 1-oxo-3-R-2H-1,2,4-benzothiadiazines, by the action of thiopheno

Preparation of 1λ4,2,4-Benzothiadiazines from N-Arylbenzamidines

N-Arylbenzamidines react with sulphenyl chlorides and N-chlorosuccinimide to give the cyclic sulphimides, 1λ4,2,4-benzothiadiazines (7), as the major products.Two examples of the analogous 1λ4,2,4-benzoselenadiazine system (8) have b