53697-48-6

Upstream product

• 68485-14-3 ethyl 2-benzyloxazole-4-carboxylate 
• 67-56-1 methanol 
• 109595-33-7 3-bromo-2-(2-phenyl-acetylamino)-2-piperidino-propionic acid methyl ester 
• 873405-41-5 2,3-dibromo-2-(2-phenyl-acetylamino)-propionic acid 
• 68485-13-2 N-((ethoxycarbonyl)methyl)phenylacetimidoyl ethyl ether 
• 4971-77-1 ethyl 2-phenylethanimidoate 
• 60084-45-9 3-bromo-2-(2-phenyl-acetylamino)-acrylic acid methyl ester 

Downstream Products

• 68485-15-4 2-benzyl-oxazole 
• 872806-24-1 2-benzyl-oxazole-4-carbonyl chloride 
• 101731-38-8 2-benzyl-oxazole-4-carboxylic acid benzylamide 
• 101285-70-5 phenyl-acetic acid-[2-(2,4-dinitro-phenylhydrazono)-ethylamide] 
• 100063-40-9 2-benzyl-oxazole-4-carboxylic acid methyl ester 
• 92580-30-8 4-(2-benzyl-oxazole-4-carbonyl)-morpholine 
• 98527-61-8 2-benzyl-oxazole-4-carbothioic acid 4-methyl-anilide 
• 97810-81-6 2-benzyl-oxazole-4-carbothioic acid anilide 
• 92580-06-8 4-(2-benzyl-oxazole-4-carbothioyl)-morpholine 
• 53697-46-4 2-benzyl-oxazole-4-carbaldehyde 
• 93323-65-0 2-benzyl-oxazole-4-carboxylic acid anilide 
• 98511-88-7 2-benzyl-oxazole-4-carboxylic acid 4-methyl-anilide 

Relevant academic research and scientific papers

Diheteroarylmethanes. 5. E-Z isomerism of carbanions substituted by 1,3-Azoles: 13C and 15N π-charge/shift relationships as source for mapping charge and ranking the electron-withdrawing power of heterocycles

Previously proposed π-charge/shift relationships have been applied to 13C and 15N shifts of the carbanions of 2-benzylazoles (thiazole, oxazole, and imidazole), their corresponding benzo-fused analogs, and bis(2-azolyl)methanes (azol

Pyridin-3-ols

New pyridin-3-ols and their N-oxides and acid addition salts, which are useful as intermediates, especially for the preparation of pharmacologically active compounds, and their preparation.