- pair C6H5NH2 and C6H5NO.
Phenylhydroxylamine should not be
confused with its
isomer α-
phenylhydroxylamine or O-
phenylhydroxylamine. This
compound can be...
- the
ammonium salt of the
conjugate base
derived from N-nitroso-N-
phenylhydroxylamine. It once was a
common reagent for the
complexation of
metal ions...
- Alternatively, the
partial hydrogenation of
nitrobenzene affords phenylhydroxylamine,
which rearranges primarily to 4-aminophenol (Bamberger rearrangement)...
- to azoxybenzene, azobenzene, nitrosobenzene, hydrazobenzene, and
phenylhydroxylamine. It has been used as a mild
oxidant in
reactions like the Skraup...
- The
Bamberger rearrangement is the
chemical reaction of
phenylhydroxylamines with
strong aqueous acid,
which will
rearrange to give 4-aminophenols. It...
-
phenols and aryl
sulfonamides n-Butyl
nitrite and
ammonia convert phenylhydroxylamine to its
nitrosamine derivative cupferron.
Likewise pyrrolidine is...
-
methemoglobinemia is
produced in
humans mainly by
another metabolite,
phenylhydroxylamine. A follow-up
paper by
Brodie and
Axelrod in 1949
established that...
- nitrobenzene. This
reaction is
proposed to
proceed via the
intermediacy of
phenylhydroxylamine and nitrosobenzene:
PhNHOH + PhNO → PhN(O)NPh + H2O
Another option...
-
Aminophenols 2-Aminophenol 3-Aminophenol 4-Aminophenol
Nicotinyl alcohol Phenylhydroxylamine Vince lactam This set
index page
lists chemical structure articles...
- Syntheses;
Collected Volumes, vol. 4, p. 148. Kamm, O. (1941). "β-
Phenylhydroxylamine".
Organic Syntheses;
Collected Volumes, vol. 1, p. 445. Ichikawa...
