Hemiaminals are tautomeric with their corresponding imine or ketone forms. They can easily equilibrate under certain conditions. Depending on the reaction conditions, the hemiaminal can convert back into the nitrone or transform into a different product.
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Benzenemethanamine, N-(1-methylethylidene)-, N-oxide
C28H22N8O6
2-tert-butyl-4-methoxy-6-[(pyridin-2-ylmethylimino)methyl]phenol
