- peroxide. In the laboratory,
azines are
typically prepared by
condensation of
hydrazine with two
equivalents of a carbonyl.
Azines are also
produced when chalcone...
- Jean-Pierre; Combroux, Jean & Delavarenne,
Serge Yvon, "Method for
preparing azines and hydrazones",
issued 1976-08-03, ****igned to
Produits Chimiques Ugine...
- itself,
hydrazones condense with a
second equivalent of a
carbonyl to give
azines: R2C=N−NH2 + R2C=O → R2C=N−N=CR2 + H2O
Hydrazones are
intermediates in the...
- Angerhofer, Cidy K.; Williams, Jean A. "Antimalarial dyes revisited: xanthenes,
azines, oxazines, and thiazine"
Antimicrobial Agents and
Chemotherapy (1995), 39(12)...
- as dimethazine, dymethazine, di(methasterone)
azine, or 2α,17α-dimethyl-5α-androstan-17β-ol-3-one
azine) is a synthetic,
orally active androgen/anabolic...
- In Hantzsch–Widman nomenclature, an
azine is an
heterocyclic compound containing a 6-membered
aromatic ring. It is an
analog of a
benzene ring in which...
- This
hydrazone condenses with one more
equivalent of ketone. The
resulting azine is
hydrolyzed to give
hydrazine and
regenerate the ketone,
methyl ethyl...
- Jamal; Ismail, Ali I. (2018). "Metal-free and FeCl3-catalyzed
synthesis of
azines and 3,5-diphenyl-1H-pyrazole from
hydrazones and/or
ketones monitored by...
- PMID 36879075. S2CID 257377020. J.
Fabian and E.
Lewars (2004). "Azabenzenes (
azines) — The
nitrogen derivatives of
benzene with one to six N atoms: Stability...
- 83–86. doi:10.7326/0003-4819-75-1-83. PMID 5091568.
Berneth H (2012). "
Azine Dyes". Ullmann's
Encyclopedia of
Industrial Chemistry. Weinheim: Wiley-VCH...
