17739-97-8 Usage
Description
(6Z)-4-methyl-6-[(4-methylphenyl)hydrazono]cyclohexa-2,4-dien-1-one is a chemical compound belonging to the cyclohexa-2,4-dien-1-one family, characterized by the presence of a hydrazone functional group. It has a molecular formula of C14H14N2O and a molecular weight of 226.27 g/mol. This yellow crystalline powder is insoluble in water but soluble in organic solvents like chloroform and ethanol. (6Z)-4-methyl-6-[(4-methylphenyl)hydrazono]cyclohexa-2,4-dien-1-one's hydrazone moiety, known for its diverse biological activities, suggests potential applications in medicinal and pharmaceutical research. Further investigation is necessary to explore its full potential and properties.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 17739-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,3 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17739-97:
(7*1)+(6*7)+(5*7)+(4*3)+(3*9)+(2*9)+(1*7)=148
148 % 10 = 8
So 17739-97-8 is a valid CAS Registry Number.
17739-97-8Relevant articles and documents
Tautomerisation in 1-(4-methylphenylazo)naphthalen-2-ol and 2-(4-methylphenylazo)-4-methylphenol: a crystallographic and NMR study.
Cross, Wendy I.,Flower, Kevin R.,Pritchard, Robin G.
, p. 834 - 853 (2007/10/03)
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. XVI. Formation of o-Hydroxyazoarenes by Condensation with o-Hydroxynitroarenes. Favorable Role of o-Hydroxyl Group in the Reaction
Okubo, Masao,Nakashima, Takanori,Shiku, Haruko
, p. 1621 - 1625 (2007/10/02)
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
Masoud, Mamdouh S.,Elnahas, H. M.,Khalil, E. A.
, p. 347 - 348 (2007/10/02)
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
