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1-(2-trifluoromethyl-benzoyl)-thiosemicarbazide is a chemical compound with the molecular formula C9H8F3N3OS. It is a derivative of thiosemicarbazide, featuring a trifluoromethyl-benzoyl group attached to the 1-position of the thiosemicarbazide molecule. 1-(2-trifluoromethyl-benzoyl)-thiosemicarbazide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new compounds with biological activity. The presence of the trifluoromethyl group enhances the lipophilicity and metabolic stability of the molecule, which can be beneficial in drug design. The compound is also of interest in the field of organic chemistry for its reactivity and the ability to form various adducts and derivatives.

7653-34-1

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7653-34-1 Usage

Structure

Thiosemicarbazide derivative with a trifluoromethyl-benzoyl group attached to the nitrogen atom

Pharmacological properties

Potential as an anti-tuberculosis agent

Biological activities

Antimicrobial, antifungal, and antitumor properties

Research and development

Promising candidate for further research and development in the field of medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 7653-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7653-34:
(6*7)+(5*6)+(4*5)+(3*3)+(2*3)+(1*4)=111
111 % 10 = 1
So 7653-34-1 is a valid CAS Registry Number.

7653-34-1Relevant academic research and scientific papers

Synthesis and biological evaluation of 1,2,4-triazole-3-thione and 1,3,4-oxadiazole-2-thione as antimycobacterial agents

Sonawane, Amol D.,Rode, Navnath D.,Nawale, Laxman,Joshi, Rohini R.,Joshi, Ramesh A.,Likhite, Anjali P.,Sarkar, Dhiman

, p. 200 - 209 (2017/07/13)

Resistance among dormant mycobacteria leading to multidrug-resistant and extremely drug-resistant tuberculosis is one of the major threats. Hence, a series of 1,2,4-triazole-3-thione and 1,3,4-oxadiazole-2-thione derivatives (4a–5c) have been synthesized and screened for their antitubercular activity against Mycobacterium tuberculosis H37Ra (H37Ra). The triazolethiones 4b and 4v showed high antitubercular activity (both MIC and IC50) against the dormant H37Ra by in vitro and ex vivo. They were shown to have more specificity toward mycobacteria than other Gram-negative and Gram-positive pathogenic bacteria. The cytotoxicity was almost insignificant up to 100?μg/ml against THP-1, A549, and PANC-1 human cancer cell lines, and solubility was high in aqueous solution, indicating the potential of developing these compounds further as novel therapeutics against tuberculosis infection.

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