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(2-(trifluoromethyl)-10H-phenothiazin-10-yl)(3,4,5-trimethoxyphenyl)methanone is a complex organic compound characterized by its unique molecular structure. It features a phenothiazine core, which is a heterocyclic compound with a tricyclic structure consisting of two benzene rings and a sulfur-containing ring. The phenothiazine ring in (2-(trifluoromethyl)-10H-phenothiazin-10-yl)(3,4,5-trimethoxyphenyl)methanone is substituted with a trifluoromethyl group at the 2-position, which imparts specific chemical properties due to the presence of three fluorine atoms. Additionally, the compound has a trimethoxyphenyl group attached to the methanone (or ketone) functional group, which is characterized by a carbonyl group (C=O) bonded to a methyl group. The trimethoxyphenyl group has three methoxy groups (-OCH3) attached to the benzene ring, further contributing to the compound's chemical reactivity and potential applications. This molecule's structure suggests it may have applications in pharmaceuticals or as a chemical intermediate, although specific uses would depend on its physical and chemical properties, which are not detailed in this summary.

2353-77-7

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2353-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2353-77-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2353-77:
(6*2)+(5*3)+(4*5)+(3*3)+(2*7)+(1*7)=77
77 % 10 = 7
So 2353-77-7 is a valid CAS Registry Number.

2353-77-7Downstream Products

2353-77-7Relevant academic research and scientific papers

Discovery of indoline derivatives that inhibit esophageal squamous cell carcinoma growth by Noxa mediated apoptosis

Fu, Dong-Jun,Li, Miaomiao,Zhang, Sai-Yang,Li, Jiang-Feng,Sha, Beibei,Wang, Longhao,Zhang, Yan-Bing,Chen, Ping,Hu, Tao

, (2019/08/27)

A series of novel indoline derivatives were synthesized and evaluated for antiproliferative activity against four selected cancer cell lines (Hela, A549, HepG2 and KYSE30). Among them, compound 20 displayed the potent inhibition activity against esophagea

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