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(2E)-2-(2,4-dimethylbenzylidene)hydrazinecarbothioamide, also known as DMTBC, is an organic compound with the molecular formula C11H14N4S. It is a yellow crystalline solid that features a benzene ring and a hydrazine group in its chemical structure. (2E)-2-(2,4-dimethylbenzylidene)hydrazinecarbothioamide is recognized for its potential applications in various scientific fields, including pharmaceuticals, agriculture, and materials science.

6292-72-4

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6292-72-4 Usage

Uses

Used in Pharmaceutical Development:
DMTBC is utilized as a reagent in the synthesis of various organic compounds, particularly those with potential pharmacological properties. Its unique structure and reactivity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Antimicrobial and Antifungal Agents:
DMTBC exhibits antimicrobial and antifungal activities, which makes it a promising candidate for the development of new pharmaceuticals aimed at treating infections caused by bacteria and fungi. Its effectiveness in combating these microorganisms can lead to the creation of novel treatments and preventative measures.
Used in Agricultural Products:
The antimicrobial and antifungal properties of DMTBC also extend to its use in agriculture, where it can be employed to protect crops from diseases and pests. This application can contribute to increased crop yields and reduced reliance on harmful chemical pesticides.
Used in Materials Science:
DMTBC's potential applications in materials science include its use in the development of new materials with specific properties, such as improved stability or reactivity. Its unique chemical structure allows for the exploration of its integration into various material systems.
Used in Industrial Processes:
(2E)-2-(2,4-dimethylbenzylidene)hydrazinecarbothioamide may also find use in various industrial processes, where its reactivity and properties can be harnessed to improve efficiency, catalyze reactions, or create new products. DMTBC's versatility positions it as a candidate for innovation across multiple industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6292-72-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6292-72:
(6*6)+(5*2)+(4*9)+(3*2)+(2*7)+(1*2)=104
104 % 10 = 4
So 6292-72-4 is a valid CAS Registry Number.

6292-72-4Relevant academic research and scientific papers

Reactions of trichloromethylarenes with hydrazine derivatives. Synthesis of 2,5-disubstituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles

Poddubnyi,Belen'kii,Krayushkin

, p. 1185 - 1188 (2007/10/03)

The effect of the solvent on the course of the reaction between trichloromethylarenes and thioacylhydrazines or acylhydrazines has been considered. In alcohols as solvents, alkyl arenecarboxylates form as a result of alcoholysis, while 2,5-disubstituted 1,3,4-thiadiazoles (1,3,4-oxadiazoles) form as minor products. In pyridine solutions, the major or sole products are those of reductive condensation, i.e., the corresponding N-substituted hydrazones of arenecarbaldehydes. 1,3,4-Thiadiazole or 1,3,4-oxadiazole derivatives are obtained in good yield when the reaction is carried out in a pyridine - alkanol mixture.

SYNTHESIS OF 2-AMINO-5-ARYL-1,3,4-THIADIAZOLES FROM TRICHLOROMETHYLARENES: THE EFFECT OF REACTION CONDITIONS

Belen'kii, Leonid,Poddubny, Igor,Krayushkin, Mikhaill

, p. 469 - 470 (2007/10/02)

The factors have been considered controlling the course of the interaction between trichloromethylarenes and thioacylhydrazines.

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