93652-48-3

Upstream product

• 87687-75-0 methyl 4-(benzyloxy)-3-hydroxybenzoate 
• 75-26-3 isopropyl bromide 
• 2150-43-8 3,4-dihydroxybenzoic acid methyl ester 
• 1002984-09-9 ethyl 4-(benzyloxy)-3-isopropoxybenzoate 
• 177429-27-5 ethyl 4-benzyloxy-3-hydroxybenzoate 
• 100-44-7 benzyl chloride 

Downstream Products

• 1574285-26-9 C₁₇H₁₉NO₃ 
• 1574285-28-1 C₂₂H₂₃NO₅ 
• 1574285-30-5 C₁₅H₁₇NO₅ 
• 1574285-32-7 C₁₆H₁₇F₂NO₅ 
• 1574285-36-1 C₁₄H₁₅F₂NO₄ 
• 1574285-38-3 C₁₄H₁₄BrF₂NO₃ 
• 1574285-40-7 2-((2-(4-difluoromethoxy-3-isopropoxyphenyl)oxazol-4-yl)methyl)isoindoline-1,3-dione 
• 1574285-43-0 C₁₄H₁₆F₂N₂O₃*ClH 
• 937782-05-3 N-({2-[4-(difluoromethoxy)-3-isopropoxyphenyl]oxazole-4-yl}methyl)-2-ethoxybenzamide 
• 104665-70-5 4-acetoxy-3-isopropoxy-benzoic acid 
• 101776-77-6 4-hydroxy-3-isopropoxy-benzoic acid diethylamide 
• 99186-66-0 4-hydroxy-3-isopropoxy-benzoic acid 

Relevant academic research and scientific papers

METHOD FOR PRODUCING OXAZOLE COMPOUND

An object of the present invention is to provide a novel method for producing an oxazole compound. The invention relates to a method for producing a compound represented by formula (1): wherein R1 is lower alkyl group or halogen substituted lower alkyl group, R2 is lower alkyl group, R5 is lower alkyl group, R11 is lower alkyl group, halogen substituted lower alkyl group or a group represented by formula: -CY2COOR12, wherein Y is a halogen atom, R12 is an alkali metal atom or lower alkyl group, Ar1 is phenyl group substituted with lower alkyl group, etc., or pyridyl group substituted with lower alkyl group, etc., X2, X3 and X9 are the same or different and are halogen atoms, X4 is a leaving group, and M is an alkali metal atom.