34905-96-9

Upstream product

• 34906-02-0 5-benzoylamino-2-phenyl-1H-pyrimidine-4,6-dione 
• 618-32-6 Benzoyl bromide 
• 88584-27-4 5-Ethoxy-2-phenyl-oxazole-4-carboxylic acid 1-amino-1-phenyl-meth-(E)-ylideneamide 
• 54644-12-1 5-ethoxy-2-phenyloxazole-4-carboxylic acid 
• 54644-14-3 2-phenyl-5-ethoxyoxazole-4-carboxylic acid chloride 
• 88584-21-8 5-(Benzimidoyl-amino)-2-phenyl-oxazole-4-carboxylic acid ethyl ester 
• 34905-95-8 C₂₄H₁₅N₃O₃ 
• 83990-33-4 5-benzylthio-2-phenyl-4-methoxycarbonyloxazole 
• 1670-14-0 benzamidine monohydrochloride 
• 54902-31-7 methyl ester of 3,3-dichloro-2-benzoylaminoacrylic acid 

Downstream Products

• 34906-03-1 7-chloro-2,5-diphenyl[1,3]oxazolo[5,4-d]pyrimidine 

Relevant academic research and scientific papers

Synthesis, in silico and in vitro Evaluation of Novel Oxazolopyrimidines as Promising Anticancer Agents

New potential bioactive oxazolopyrimidines have been synthesized using two main approaches: the pyrimidine ring annulation on a functionalized oxazole and the benzoyl bromide trimerization followed by rearrangement and formation of the oxazolo[5,4-d]pyrim

Synthesis of methyl 2-aryl-5-chlorosulfonyl-1,3-oxazole-4-carboxylates and their reactions with amines and amidines

Previously unknown methyl 2-aryl-5-chlorosulfonyl-1,3-oxazole-4-carboxylates have been synthesized. Their reactions with amines and amidines have yielded the corresponding sulfonamides and 6H,7H-[1,3]oxazolo-[5,4-d]pyrimidin-7-ones.