4123-32-4

Upstream product

• 333-20-0 potassium thioacyanate 
• 62-53-3 aniline 
• 728-84-7 2-bromo-1,3-diphenylpropane-1,3-dione 
• 103-85-5 monophenylthiourea 
• 7471-86-5 methyl benzimidate 
• 72149-84-9 1-(methoxyphenylmethylene)-3-phenylthiourea 
• 70-11-1 α-bromoacetophenone 
• 103-72-0 phenyl isothiocyanate 
• 50458-37-2 N,N-diethylbenzamidine 
• 1670-14-0 benzamidine monohydrochloride 
• 39536-03-3 N-phenylthiocarbamoylbenzamidine 
• 120-46-7 1,3-diphenylpropanedione 
• 4571-27-1 2-chloro-1,3-diphenyl-propane-1,3-dione 
• 4276-55-5 N-(5-benzoyl-4-phenyl-thiazol-2-yl)-N-phenyl-acetamide 

Downstream Products

• 4276-54-4 [2-(N-nitroso-anilino)-4-phenyl-thiazol-5-yl]-phenyl-methanone 
• 4276-55-5 N-(5-benzoyl-4-phenyl-thiazol-2-yl)-N-phenyl-acetamide 

Relevant academic research and scientific papers

One pot synthesis and antimicrobial activity of substituted 2-Aminothiazoles

In this work, we described a preparation of substituted 2-Aminothiazoles by two different methods using a one-pot procedure and starting from methoxymethylene-3-Aryl-thiourea (2). The synthesized 2-Aminothiazoles (5a-h) were characterized on the basis of

An efficient one-pot synthesis of functionally diverse 2-aminothiazoles from isothiocyanates, amidines/guanidines and halomethylenes

An efficient one-pot method for the synthesis of 2-aminothiazoles using simple starting materials like isothiocyanates, amidines/guanidines and various halomethylenes is reported. The synthesis of 2-aminothiazoles involves reactions such as nucleophilic a

Facile Synthesis of Aminothiazoles

The reaction of thioureas with ketones in the presence of N-bromosuccinimide furnishes 2-aminothiazoles.The method is quick, convenient and versatile.