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3-(Trifluoromethyl)-10H-phenothiazine is a chemical compound with the molecular formula C14H8F3NS. It is a derivative of phenothiazine, a heterocyclic compound with a tricyclic structure consisting of two benzene rings and a thiazine ring. The presence of a trifluoromethyl group (-CF3) at the 3-position of the phenothiazine core imparts unique properties to 3-(trifluoromethyl)-10H-phenothiazine. This fluorinated phenothiazine is known for its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, due to its electronic and steric effects. The trifluoromethyl group can influence the compound's reactivity, stability, and lipophilicity, making it a subject of interest in chemical research and development.

397-50-2

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397-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 397-50-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 397-50:
(5*3)+(4*9)+(3*7)+(2*5)+(1*0)=82
82 % 10 = 2
So 397-50-2 is a valid CAS Registry Number.

397-50-2Downstream Products

397-50-2Relevant academic research and scientific papers

Radical Route to 1,4-Benzothiazine Derivatives from 2-Aminobenzenethiols and Ketones under Transition-Metal-Free Conditions

Lin, Ya-mei,Lu, Guo-ping,Wang, Rong-kang,Yi, Wen-bin

supporting information, p. 6424 - 6427 (2016/12/23)

Transition-metal-free radical access to 1,4-benzothiazine derivatives from o-aminobenzenethiols is disclosed. This procedure is available for various ketones including α,β-unsaturated, cyclic, linear, and fluoroalkyl ketones to generate a number of 1,4-benzothiazines, which exist in numerous bioactive and natural molecules, rendering this protocol attractive to both synthetic and medicinal chemistry.

Potassium carbonate-mediated tandem C-S and C-N coupling reaction for the synthesis of phenothiazines under transition-metal-free and ligand-free conditions

Wu, San,Hu, Wei-Ye,Zhang, Song-Lin

, p. 24257 - 24260 (2016/03/15)

An efficient potassium carbonate-mediated tandem C-S and C-N coupling reaction between N-(2-iodophenyl)acetamides and 2-halo-benzenethiols has been developed. This protocol affords a simple and efficient approach for the construction of phenothiazine derivatives without the need for addition of transition-metal catalyst or ligand for the first time. Furthermore, the reaction can be easily performed on a large scale.

Synthesis of phenothiazines via ligand-free CuI-catalyzed cascade C-S and C-N coupling of aryl ortho-dihalides and ortho-aminobenzenethiols

Dai, Chuan,Sun, Xiaofei,Tu, Xingzhao,Wu, Li,Zhan, Dan,Zeng, Qingle

experimental part, p. 5367 - 5369 (2012/06/04)

A ligand-free CuI-catalyzed cascade C-S and C-N cross coupling of (hetero)aryl ortho-dihalides and ortho-aminobenzenethiols has been developed, and various phenothiazines were synthesized with excellent regioselectivity. A possible mechanism is proposed for the cascade coupling.

Assembly of substituted phenothiazines by a sequentially controlled CuI/L-proline-catalyzed cascade C-S and C-N bond formation

Dawei, Ma.,Geng, Qian,Zhang, Hui,Jiang, Yongwen

supporting information; experimental part, p. 1291 - 1294 (2010/05/17)

(Chemical equation presented) In the pro-line of fire: A general and efficient cascade reaction approach to substituted phenothiazines, which relies on controlled sequential Cul/L-prolinecatalyzed C-S and C-N bond formations, is described. DMSO = dimethylsulfoxide.

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