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3,5-dimethyl-4-[(4-methylphenyl)hydrazono]-4H-pyrazole is a complex organic compound with the molecular formula C13H15N3. It is a derivative of pyrazole, a heterocyclic compound with a five-membered ring containing three carbon atoms and two nitrogen atoms. The structure of 3,5-dimethyl-4-[(4-methylphenyl)hydrazono]-4H-pyrazole is characterized by two methyl groups attached to the 3rd and 5th carbon atoms of the pyrazole ring, and a hydrazono group connected to the 4th carbon atom. The hydrazono group is formed by a nitrogen atom double-bonded to the 4-methylphenyl group, which is a benzene ring with a methyl group attached to the 4th carbon. 3,5-dimethyl-4-[(4-methylphenyl)hydrazono]-4H-pyrazole is of interest in chemical research due to its potential applications in various fields, such as pharmaceuticals and materials science, and its unique chemical properties.

3656-06-2

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3656-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3656-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3656-06:
(6*3)+(5*6)+(4*5)+(3*6)+(2*0)+(1*6)=92
92 % 10 = 2
So 3656-06-2 is a valid CAS Registry Number.

3656-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3,5-dimethylpyrazol-4-ylidene)amino]-4-methylaniline

1.2 Other means of identification

Product number -
Other names 4-(4'-Tolylazo)-3,5-dimethyl-pyrazol

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:3656-06-2 SDS

3656-06-2Relevant academic research and scientific papers

Solvent-free synthesis of novel (E)-2-(3,5-dimethyl-4-(aryldiazenyl)-1H-pyrazol-1-yl)-4-arylthiazoles: Determination of their biological activity

Kaur, Kamalneet,Kumar, Vinod,Beniwal, Vikas,Kumar, Vikas,Aneja,Sharma, Vishal,Jaglan, Sundeep

, p. 3863 - 3875 (2015)

In search of novel biologically active azoles, some new (E)-2-(3,5-dimethyl-4-(aryldiazenyl)-1H-pyrazol-1-yl)-4-arylthiazoles 3a-p have been synthesized via Hantzsch thiazole approach under greener, mild and solvent-free conditions. Structures of all comp

Synthesis of mycostatics based on 4-aryldiazenyl-3,5-dimethylpyrazoles

Burgart, Ya. V.,Evstigneeva, N. P.,Gerasimova, N. A.,Ivanova, A. E.,Khudina, O. G.,Saloutin, V. I.

, p. 1124 - 1130 (2021/07/21)

The condensation of 3-arylhydrazinylidenepentane-2,4-diones with hydrazine hydrate, 2-hydroxyethylhydrazine, benzylhydrazine hydrochloride, and 4-hydrazinylbenzenesulfonamide hydrochloride gave 4-aryldiazenyl-3,5-dimethylpyrazoles. An alternative route to

Evaluation of Substituent Effect in Z -Isomer Stability of Arylazo-1 H -3,5-dimethylpyrazoles: Interplay of Steric, Electronic Effects and Hydrogen Bonding

Devi, Sudha,Saraswat, Mayank,Grewal, Surbhi,Venkataramani, Sugumar

supporting information, p. 4307 - 4322 (2018/04/26)

The electronic and steric effects of aryl substituents and the influence of hydrogen bonding in Z-isomer stability of phenylazopyrazole derivatives have been investigated. In this regard, 38 substituted phenylazopyrazole derivatives and 6 N-methyl phenyla

Studies with Polyfunctionally Substituted Heterocycles: New Synthesis of Pyrido[5′,4′:2,3][1,3,4]oxadiazolo[3,2-a]pyridine; Pyridazine; 1,3,4-Oxadiazole; and Pyrazolo[1,5-a]Pyrimidine Derivatives

Barsy, Magda A.,Elmaghraby, Mohammed A.,Ahmed, Salwa M.

, p. 655 - 658 (2007/10/03)

Cyanoacetohydrazide 1a reacts with 2-arylhydrazoketons 2a,b and 3a,b in refluxing ethanol to yield pyrido[5′,4′:2,3][1,3,4]oxadiazolo[3,2-a]pyridine and pyridazine derivatives; in the absence of solvent pyrazolo[1,5-a]pyrimidine derivatives were obtained.

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