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17739-97-8

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17739-97-8 Usage

General Description

The chemical compound "(6Z)-4-methyl-6-[(4-methylphenyl)hydrazono]cyclohexa-2,4-dien-1-one" is a member of the cyclohexa-2,4-dien-1-one family, featuring a hydrazone functional group. It has a molecular formula of C14H14N2O and a molecular weight of 226.27 g/mol. The compound exists as a yellow crystalline powder and is insoluble in water but soluble in organic solvents such as chloroform and ethanol. The chemical may have potential applications in medicinal and pharmaceutical research due to the presence of the hydrazone moiety, which is known to exhibit diverse biological activities. Further research and testing may be warranted to explore the potential uses and properties of this compound.

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.

17739-97-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-5,4'-dimethylazobenzene

1.2 Other means of identification

Product number -
Other names Phenol, 4-methyl-2-[(4-methylphenyl)azo]-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17739-97-8 SDS

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

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