19959-13-8

Upstream product

• 2010-06-2 2-Amino-4-phenylthiazole 
• 123-11-5 4-methoxy-benzaldehyde 
• 98-86-2 acetophenone 

Downstream Products

• 67948-08-7 N-[3-isopropyl-2-(4-methoxy-phenyl)-4-oxo-1-(4-phenyl-thiazol-2-yl)-azetidin-3-yl]-phthalimide 
• 67947-93-7 N-[2-(4-methoxy-phenyl)-3-methyl-4-oxo-1-(4-phenyl-thiazol-2-yl)-azetidin-3-yl]-phthalimide 
• 1445009-43-7 N,5-bis(4-methoxybenzyl)-4-phenylthiazol-2-amine 
• 67947-78-8 N-[2-(4-methoxy-phenyl)-4-oxo-1-(4-phenyl-thiazol-2-yl)-azetidin-3-yl]-phthalimide 
• 72192-73-5 3-(2-chloro-phenoxy)-4-(4-methoxy-phenyl)-1-(4-phenyl-thiazol-2-yl)-azetidin-2-one 
• 72192-74-6 4-(4-methoxy-phenyl)-3-(4-nitro-phenoxy)-1-(4-phenyl-thiazol-2-yl)-azetidin-2-one 

Relevant academic research and scientific papers

Insecticidal Evaluation and [4+2] Aza-Diels-Alder Synthesis of 3,7-Diaryl-6,7-dihydro-5H-6-substituted Thiazolo[3,2-a]pyrimidin-5-ones Under Coupled Ultrasonic Irradiation and PTC

(Chemical Equation Presented) A series of 3,7-diaryl-6,7-dihydro-5H-6-substituted-thiazolo[3,2-a]pyrimidin-5-ones (3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j) were synthesized by the [4+2] cycloaddition reaction of 2-arylideneamino-4-arylthiazoles (2a-j) with

Design, synthesis, biological evaluation of thiazolyl schiff base derivatives as novel anti-inflammatory agents

A series of new 4-(4-substitutedphenyl)-N-(4-substitutedbenzylidene)- thiazol-2-amine derivatives 5a-l has been synthesized and evaluated for their anti-inflammatory and analgesic activities at a dose of 50 mg/kg p.o. The most active compounds 5a, 5j have been subjected to acute ulcerogenesis study at a dose of 150 mg/kg. The structure of all these compounds have been established on the basis of spectral (IR, 1H NMR data) studies.

Formation of azomethines from 2-aminothiazoles and (heterocyclic) aromatic aldehydes

Reexamination of previous work and new studies show that the reactions of 2-aminothiazoles with (heterocyclic) aromatic aldehydes are not straightforward; there are wide divergencies in behaviour between the various amine-aldehyde pairs. Simple efficient