156027-96-2

Upstream product

• 156028-04-5 α,α-dideuterio-p-methoxybenzyl benzohydroxamate 
• 100-09-4 4-methoxybenzoic acid 
• 35693-16-4 α,α-dideuterio-p-methoxybenzyl bromide 
• 35693-15-3 p-methoxyphenylmethanol-1,1-d2 
• 127-09-3 sodium acetate 

Relevant academic research and scientific papers

Reactive Intermediates from the Solvolysis of Mutagenic O-Alkyl N-Acetoxybenzohydroxamates

Mutagenic O-(para-substituted benzyl) N-acetoxybenzohydroxamates undergo acid-catalysed solvolysis in aqueous acetonitrile but three is a change in mechanism from AA11 to E1 on going from para electron-withdrawing substituents to para +M electron-donating groups.The former permit the formation of a discrete nitrenium ion intermediate whereas the latter promote a concerted elimination of a resonance stabilized benzyl carbocation.