70027-43-9

Basic information

• Product Name: Carbamic acid, (5-phenyl-1,3,4-thiadiazol-2-yl)-, ethyl ester
• CAS NO: 70027-43-9
• Molecular Formula: C11H11N3O2S
• Molecular Weight: 249.293
• Mol File: 70027-43-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (5-phenyl-1,3,4-thiadiazol-2-yl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (5-phenyl-1,3,4-thiadiazol-2-yl)-, ethyl ester(70027-43-9)
• EPA Substance Registry System: Carbamic acid, (5-phenyl-1,3,4-thiadiazol-2-yl)-, ethyl ester(70027-43-9)

Safety Data

• Hazardous Substances Data: 70027-43-9(Hazardous Substances Data)

Upstream product

• 2002-03-1 2-amino-5-phenyl-1,3,4-thiadiazole 
• 541-41-3 chloroformic acid ethyl ester 
• 1147550-11-5 ammonium thiocyanate 
• 613-94-5 benzoic acid hydrazide 
• 65-85-0 benzoic acid 
• 1627-73-2 1-benzylidene thiosemicarbazide 
• 62441-46-7 (N'-benzimidoyl-hydrazinothiocarbonyl)-carbamic acid ethyl ester 
• 16182-04-0 Ethoxycarbonyl isothiocyanate 
• 53970-37-9 benzenecarboximidohydrazide hydroiodide 

Downstream Products

• 2002-03-1 2-amino-5-phenyl-1,3,4-thiadiazole 

Relevant articles and documents

Design, synthesis and pharmacological evaluation of carboxamide and carbothioamide derivatives of 1,3,4-thiadiazole as the inhibitors of acetylcholinesterase and oxipiperazine)ative stress for the management of cognitive debility

Acetylcholinesterase has been a promising target for the development of putative therapeutics against cognitive decline. The deleterious effect of oxidative stress on the learning and memory paradigms of an individual has also been well documented. In vie

Synthesis of 6-Aroylimino-2-aryl-1,3,4-thiadiazolothiadiazolines

Reaction of 2-amino-5-aryl-1,3,4-thiadiazoles (V) with aroyl isothiocyanates gives 2-aroylamino-5-aryl-1,3,4-thiadiazoles (VII) and N-aroyl-N'-(5-aryl-1,3,4-thiadiazol-2-yl)thioureas (VIII).Contrary to earlier reports, cyclisation of VIII in the presence of PCl5 in POCl3 yields 6-aroylimino-2-aryl-1,3,4-thiadiazolo-thiadiazolines (X).Cyclisation of VIII in the presence of other oxidising agents also leads to X.