-
hydrazones to
hydrazines present a
clean way to
produce 1,1-dialkylated
hydrazines. In a
related reaction, 2-cyanopyridines
react with
hydrazine to form amide...
-
degree of substitution.
Hydrazines belonging to the same
group behave similarly in
their chemical properties.
Monosubstituted hydrazines and so-called asymmetrically...
-
unrelated MAOI
introduced around the same time as the
hydrazines, was
originally advertised as non-
hydrazine as a
result of its
diminished propensity for causing...
-
Hydrazine nitrate is an
inorganic compound with the
chemical formula N2H4·HNO3. It has
usage in
liquid explosives as an oxidizer. It
exists in two crystalline...
-
Hydrazine sulfate, more
properly hydrazinium hydrogensulfate, is a salt of the
cation hydrazinium and the
anion bisulfate (hydrogensulfate), with the...
-
Hydrazine oxidoreductase (EC 1.7.99.8, HAO (ambiguous)) is an
enzyme with
systematic name
hydrazine:acceptor oxidoreductase. This
enzyme catalyses the...
- (isopropylidenehydrazine) is the
product of
condensation of
acetone and
hydrazine, as
typical for
hydrazone formation. It is an
intermediate in the synthesis...
-
first prepared by Emil Fischer, who
discovered and
named the
class of
hydrazines, by
reducing N-Nitrosodimethylamine with zinc in
boiling acetic acid....
- The Olin
Raschig process is a
chemical process for the
production of
hydrazine. The main
steps in this process,
patented by
German chemist Friedrich Raschig...
-
shown to
reduce hydrazine toxicity from
phenelzine and, in contrast, the
pyridoxal form has been
shown to
increase the
toxicity of
hydrazines. Phenelzine...
