65102-54-7

Upstream product

• 76-39-1 2-nitro-2-methylpropanol 
• 98-88-4 benzoyl chloride 
• 19312-06-2 4,5-dihydro-4,4-dimethyl-2-phenoxazole 

Downstream Products

• 63829-80-1 C₁₈H₁₉NO₃ 
• 63829-78-7 2-(Hydroxylamino)-2-methylpropyl benzoate 
• 65-85-0 benzoic acid 
• 84966-45-0 1-Benzoyloxy-2-methyl-N-(5-piperidinofurfuryliden)-2-propanamin-N-oxid 
• 84966-46-1 1-Benzoyloxy-N-furfuryliden-2-methyl-2-propanamin-N-oxid 

Relevant academic research and scientific papers

Oxidative cleavage of aryl oxazolines using Methyl(trifluoromethyI)dioxirane generated in situ

Oxidative cleavage of aryl oxazoline 2 using methyl(trifluoromethyl)dioxirane la generated in situ provides the intermediate nitro-ester 8, which undergoes a basic hydrolysis to furnish benzoic acid 11. Even the hindered oxazoline 7 can be cleaved smoothly to afford 3,3'-dimethyl-2,2'-diphenic acid 16. All substituted benzoic acids 11-16 can be isolated in excellent yields (80-95 %).

Ring-Chain Isomerism of N-(2-Hydroxyalkyl)nitrones, III. Nitrones of 2-Furancarbaldehydes

The ring-chain isomerism of N-(2-hydroxyalkyl)nitrones 3, obtained from 2-furancarbaldehyde and its 5-dialkylamino and 5-nitro derivatives, is studied by acylation of 3 with diphenylborinic acid, carboxylic acids, and isocyanates.Dependent on the kind of