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7382-40-3

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7382-40-3 Usage

General Description

2-(4-Methylphenyl)-1-hydrazinecarbothioamide is a chemical compound with the molecular formula C9H12N4S. It is a hydrazine derivative with a thiocarboxamide group, and the presence of a methylphenyl group on the nitrogen atom. 2-(4-METHYLPHENYL)-1-HYDRAZINECARBOTHIOAMIDE is used in various chemical and pharmaceutical applications, including as a building block in organic synthesis. It has demonstrated potential as a pharmaceutical intermediate and may be used in the development of new drugs. Additionally, it may have applications in agricultural and industrial processes. However, further research is needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 7382-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7382-40:
(6*7)+(5*3)+(4*8)+(3*2)+(2*4)+(1*0)=103
103 % 10 = 3
So 7382-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N3S/c1-6-2-4-7(5-3-6)10-11-8(9)12/h2-5,10H,1H3,(H3,9,11,12)

7382-40-3Relevant articles and documents

Discovery of novel hybrids of diaryl-1,2,4-triazoles and caffeic acid as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase for cancer therapy

Cai, Hao,Huang, Xiaojing,Xu, Shengtao,Shen, Hao,Zhang, Pengfei,Huang, Yue,Jiang, Jieyun,Sun, Yijun,Jiang, Bo,Wu, Xiaoming,Yao, Hequan,Xu, Jingyi

, p. 89 - 103 (2015/12/04)

Inflammation plays a key role in cancer initiation and propagation. Cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), two important enzymes in inflammatory responses are up-regulated in various tumor types. Dual inhibition of COX-2 and 5-LOX constitutes a rational concept for the design of more efficacious anti-tumor agents with an improved safety profile. We have previously reported a series of diaryl-1,2,4-triazole derivatives as selective COX-2 inhibitors. Herein, we hybridized the diaryl-1,2,4-triazoles with caffeic acid (CA) which was reported to display 5-LOX inhibitory and anti-tumor activities, affording a novel class of COX-2/5-LOX dual inhibitors as anti-tumor drug candidates. Most of these compounds exhibited potent COX-2/5-LOX inhibitory and antiproliferative activities in vitro. And the most potent compound 22b could significantly inhibit tumor growth in vivo. Furthermore, mechanistic investigation showed that the representative compound 15c blocked cell cycle in G2 phase and induced apoptosis in human non-small cell lung cancer A549 cells in a dose-dependent manner. Our preliminary investigation results would provide new clues for the cancer theatment with COX-2/5-LOX dual inhibitors.

Structure-activity studies of 4-phenyl-substituted 2′-benzoylpyridine thiosemicarbazones with potent and selective anti-tumour activity

Lukmantara, Adeline Y.,Kalinowski, Danuta S.,Kumar, Naresh,Richardson, Des R.

, p. 6414 - 6425 (2013/09/23)

2′-Benzoylpyridine thiosemicarbazones (BpT) are effective iron chelators and display potent anti-proliferative activity against tumour cells. In order to gain greater insight into the structure-activity relationships of the BpT chelators, ten new analogue

Anthelmintic 2 arylhydrazino and 2 arylazo 2 thiazolines

Wu,Waksmunski,Hoff,Fisher,Egerton,Patchett

, p. 1150 - 1153 (2007/10/05)

Some 2 arylhydrazino and 2 arylazo 2 thiazolines were synthesized for anthelmintic testing. The most potent compound, 2 (o tolylazo) 2 thiazoline, was orally effective in sheep against a broad range of helminths.

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