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3,4-Dimethylphenylhydrazine hydrochloride is a hydrazine class organic compound, characterized by its light yellow crystalline powder form and solubility in water and organic solvents. It is a versatile chemical with applications in pharmaceutical and agrochemical synthesis, as well as in scientific research for studying the toxic effects of hydrazine compounds on biological systems. However, it is also recognized as a carcinogen, mutagen, and teratogen, necessitating careful handling in laboratory settings.

13636-53-8

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13636-53-8 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3,4-Dimethylphenylhydrazine hydrochloride is used as a precursor in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used in Scientific Research:
3,4-Dimethylphenylhydrazine hydrochloride is used as a model compound in scientific research for studying the toxic effects of hydrazine compounds on biological systems, aiding in the understanding of their mechanisms of action and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 13636-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13636-53:
(7*1)+(6*3)+(5*6)+(4*3)+(3*6)+(2*5)+(1*3)=98
98 % 10 = 8
So 13636-53-8 is a valid CAS Registry Number.

13636-53-8Relevant academic research and scientific papers

Synthesis of new 1-(3,4-dimethylphenyl)-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-one derivatives

Zhidkov,Kutkin,Fetisova,Zverev,Zaraeva,Gorokhov,Chubarova

, p. 592 - 598 (2017/06/06)

New substituted pyrazolo[3,4-d]pyrimidin-4-ones have been synthesized as a result of a series of transformations including hydrolysis of ethyl 5-amino-1H-pyrazole-4-carboxylates, cyclization of the carboxylic acids thus obtained to pyrazolo[3,4-d][1,3]oxazin-4(1H)-ones, and treatment of the latter with substituted anilines. The final pyrazolo[3,4-d]pyrimidin-4-one derivatives can also be synthesized from 5-(arylamido)-1H-pyrazole-4-carboxylic acids in the presence of a catalytic amount of anhydrous zinc(II) chloride.

Synthesis and biological evaluation of benzimidazole phenylhydrazone derivatives as antifungal agents against phytopathogenic fungi

Wang, Xing,Chen, Yong-Fei,Yan, Wei,Cao, Ling-Ling,Ye, Yong-Hao

, (2016/12/03)

A series of benzimidazole phenylhydrazone derivatives (6a-6ai) were synthesized and characterized by 1H-NMR, ESI-MS, and elemental analysis. The structure of 6b was further confirmed by single crystal X-ray diffraction as (E)-configuration. All the compounds were screened for antifungal activity against Rhizoctonia solani and Magnaporthe oryzae employing a mycelium growth rate method. Compound 6f exhibited significant inhibitory activity against R. solani and M. oryzae with the EC50 values of 1.20 and 1.85 μg/mL, respectively. In vivo testing demonstrated that 6f could effectively control the development of rice sheath blight (RSB) and rice blast (RB) caused by the above two phytopathogens. This work indicated that the compound 6f with a benzimidazole phenylhydrazone scaffold could be considered as a leading structure for the development of novel fungicides.

Pyrazol-4-acetic acid compounds

-

, (2008/06/13)

Pyrazol-4-acetic acid compounds, such as substituted pyrazol-4-acetic acid, its esters, amides, nitriles and their pharamaceutically acceptable salts and method for the preparation of these compounds are disclosed. The novel compounds are useful analgesics, anti-inflammatory, and antipyretics.

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