17739-97-8

Usage

Uses

Used in Pharmaceutical Research:
(6Z)-4-methyl-6-[(4-methylphenyl)hydrazono]cyclohexa-2,4-dien-1-one is used as a compound in pharmaceutical research for its potential medicinal applications due to the presence of the hydrazone functional group, which is known to exhibit various biological activities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6Z)-4-methyl-6-[(4-methylphenyl)hydrazono]cyclohexa-2,4-dien-1-one is used as a starting material or a structural component for the development of new drugs, leveraging the hydrazone group's ability to interact with biological targets.
Used in Chemical Synthesis:
(6Z)-4-methyl-6-[(4-methylphenyl)hydrazono]cyclohexa-2,4-dien-1-one is used as an intermediate in the synthesis of more complex organic compounds, taking advantage of its solubility in organic solvents and reactivity.
Used in Analytical Chemistry:
(6Z)-4-methyl-6-[(4-methylphenyl)hydrazono]cyclohexa-2,4-dien-1-one can be used in analytical chemistry as a reference material or for the development of new analytical methods, given its distinct chemical properties and solubility profile.

Upstream product

• 106-49-0 p-toluidine 
• 58010-91-6 4-methyl-2-p-tolylazo-aniline 
• 62569-07-7 diphenyl (p-tolyl)phosphoramidate 
• 106-44-5 p-cresol 
• 99404-80-5 4-Methyl-2-(p-tolyl-NNO-azoxy)-phenol 
• 7647-01-0 hydrogenchloride 
• 2028-84-4 p-methylbenzenediazonium chloride 
• 288-32-4 1H-imidazole 
• 101870-18-2 toluene-4-diazonium ; hydroxide 
• 119-33-5 4-methyl-2-nitrophenol 
• 459-44-9 4-methylbenzenediazonium tetrafluoroborate 
• 57573-52-1 4-methylbenzene diazonium 

Downstream Products

• 6623-41-2 2-amino-4,5-dimethylphenol 
• 78267-40-0 2-Methyl-2-(4-methyl-2-p-tolylazo-phenoxy)-propionic acid 
• 16560-94-4 bis(2-{4-methyl-benzeneazo}-1-hydroxy-4-methyl-benzene)-cobalt(II) 
• 335001-40-6 Os(P(C₆H₅)3)2Br(CH₃C₆H₃N₂C₆H₃(CH₃)O) 
• 226999-85-5 [Ru(CH₃COCHCOCH₃)(CH₃C₆H₃(O)N₂C₆H₄CH₃)2] 
• 874298-54-1 carbonylhydrido(2-(4'-methylphenylazo)-4-methylphenolato-N⁽¹⁾,O)bis(triphenylphosphine)ruthenium 
• 874298-59-6 carbonyl(2-(4'-methylphenylazo)-4-methylphenolato^(2-)-C(2'),N⁽¹⁾,O)bis(triphenylphosphine)ruthenium 
• 1006709-32-5 [Ru(OC₆H₃(CH₃)N₂C₆H₃CH₃)(CO)(As(C₆H₅)3)2] 
• 1073540-50-7 CoCl(P(CH₃)3)2(OC₆H₃(CH₃)NNC₆H₃CH₃)*CH₃C₆H₄NH₂ 
• 330685-07-9 [Rh(P(C₆H₅)3)2(CH₃C₆H₃N₂OC₆H₃CH₃)Cl] 
• 110078-23-4 [RuCl(triphenylphosphine)2(4-methyl-2-(p-tolyldiazenyl)phenol(-2H))] 
• 652132-00-8 [Ir(P(C₆H₅)3)2(CH₃C₆H₃N₂C₆H₃(CH₃)O)(H)] 
• 652131-99-2 [Ir(P(C₆H₅)3)2(CH₃C₆H₄N₂C₆H₃(CH₃)O)(H)2] 
• 652131-98-1 [Ir(P(C₆H₅)3)2(CH₃C₆H₄N₂C₆H₃(CH₃)O)(H)Cl] 

Relevant academic research and scientific papers

Tautomerisation in 1-(4-methylphenylazo)naphthalen-2-ol and 2-(4-methylphenylazo)-4-methylphenol: a crystallographic and NMR study.

1-(4-methylphenylazo)naphthalen-2-ol 1 and 2-(4-methylphenylazo)-4-methylphenol 3 have been converted to their acetic acid esters 2 and 4 by treatment with NaH followed by acetyl chloride in good yield. Compounds 2, 3 and 4 have been structurally characte

Aryliminodimagnesium Reagents. XIX. Effects of Miscellaneous Metal Halides on Oxidative Self-Coupling of the Reagent, and on Its Condensation with Nitrobenzene. A New Preparative Route to o,o'-Dihydroxyazobenzene

Fourteen metal halides (MXn) were each added to the solution of aryliminodimagnesium (p-RC6H4N(MgBr)2, IDMg) in tetrahydrofuran, and the effect of MXn on relative yields of products was examined in the following three IDMg reactions: (A) oxidative coupling leading to symmetrical azobenzene, (B) condensation with nitrobenzene, and (C) condensation with o-hydroxy-substituted (o-HO) nitrobenzene.Reaction A was promoted by addition of CuCl2, and the yield of azoxybenzenes in reaction B was improved by addition of NiCl2 or CdCl2.Reaction C was similarly modified by addition of CdCl2 so as to improve the yield of o-HO-azoxybenzenes.Their acetyl derivatives underwent a facile photoinduced migration of azoxy oxygen and were successively hydrolyzed to afford bidentate chelating agents, o,o'-(HO)2-azobenzenes.

Aryliminodimagnesium Reagents. XVI. Formation of o-Hydroxyazoarenes by Condensation with o-Hydroxynitroarenes. Favorable Role of o-Hydroxyl Group in the Reaction

Hydroxy(HO)-azoxy and -azoarenes were formed by condensation of ArN(MgBr)2 with o-, m-, and p-HO-nitrobenzenes; nuclear substitution took place as a minor or a major pathway. o-HO-azobenzene was obtained in sufficiently high yield.Relative yields of the products varied according to the position of HO group and reaction conditions.The yield variation was explained by the effects of relative efficiency of single electron transfer, ?-complexation, and cooperation of reagent molecules.

Substituent Effects on Stability of Complexes of Iron(III), Cobalt(II), Nickel(II) and Copper(II) with Azocresols

The complex formation between substituted azocresols and iron(III), cobalt(II), nickel(II) and copper(II) have been studied potentiometrically in 50percent (v/v) aq ethanol at 25 deg C and μ=0.1.The stability constants of the complexes follow Irving-Willi