69135-70-2

Upstream product

• 147-93-3 Thiosalicylic acid 
• 635-21-2 5-chloroanthranilic acid 
• 86672-62-0 Potassium; 2-amino-5-chloro-benzoate 
• 20324-50-9 5-chloro-2-mercapto-benzoic acid 
• 56-23-5 tetrachloromethane 
• 7782-50-5 chlorine 
• 7705-08-0 iron(III) chloride 

Downstream Products

• 66949-65-3 2-(4-Acetylphenylthio)-5-chlorbenzoesaeure 
• 92435-09-1 <2-Carbamoyl-4-chlor-phenylmercapto>-essigsaeure-anilid 
• 93257-46-6 <2-Carbamoyl-4-chlor-phenylmercapto>-essigsaeure-butylamid 
• 90537-38-5 <2-Carbamoyl-4-chlor-phenylmercapto>-essigsaeure 
• 90649-53-9 <2-Carbamoyl-4-chlor-phenylmercapto>-essigsaeure-amid 
• 89692-52-4 5-Chlor-2-mercapto-benzoesaeure-amid 
• 16505-54-7 2,2'-dithiobis(5-chlorobenzamide) 
• 89756-81-0 7-chloro-3-(2,4-dichlorophenyl)-1-(4-morpholinylamino)-9H-thioxanthen-9-one 
• 89756-85-4 7'-chloro-3'-(2,4-dichlorophenyl)-3',4'-dihydrospiro<1,3-dioxolane-2,1'<1H>thioxanthen>-9'(2'H)-one 10',10'-dioxide 
• 89756-78-5 7-chloro-3-(2,4-dichlorophenyl)-1-<<(3-dimethylamino)propyl>amino>-3,4-dihydro-9H-thioxanthen-9-one 
• 89756-79-6 7-chloro-3-(2,4-dichlorophenyl)-1-<<(3-dimethylamino)propyl>amino>-9H-thioxanthen-9-one 
• 78468-94-7 C₁₈H₁₈Cl₂N₂O₄S₂ 
• 64015-89-0 2-chlorocarbonyl-4-chlorophenylsulphenyl chloride 
• 64015-88-9 5-chloro-2,2'-dithio(bisbenzoyl chloride) 

Relevant academic research and scientific papers

Endothelin receptor antagonists: Synthesis and structure-activity relationships of substituted benzothiazine-1,1-dioxides

The development of benzothiazine-1,1-dioxide derivatives as a new structural class of potent endothelin receptor antagonists is described. Structure-activity relationships (SAR) revealed that PD164800 (1) is a potent antagonist of the ET(A) receptor subtype. Copyright (C) 1998 Elsevier Science Ltd.

3,3'-Bis-methylene-1,3-benzo-thiazine compounds

3,3'-Bis-Methylene-1,3-benzothiazine compounds are inhibitors of phenylethanolamine N-methyl-transferase.