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2-(2-Phenylethylsulfanyl)aniline is an organic compound with the chemical formula C14H15NS. It is a derivative of aniline, featuring a phenylethylsulfanyl group attached to the 2-position of the aniline molecule. 2-(2-phenylethylsulfanyl)aniline is characterized by its aromatic structure, with a benzene ring attached to an ethyl group that further connects to a sulfur atom, which in turn is bonded to the aniline moiety. It is a colorless to pale yellow liquid with a distinct aromatic odor. This chemical is primarily used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and structural properties. It is important to handle 2-(2-phenylethylsulfanyl)aniline with care, as it may have potential health and environmental impacts, and is typically used in a controlled laboratory setting or industrial application.

6397-34-8

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6397-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6397-34-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6397-34:
(6*6)+(5*3)+(4*9)+(3*7)+(2*3)+(1*4)=118
118 % 10 = 8
So 6397-34-8 is a valid CAS Registry Number.

6397-34-8Relevant academic research and scientific papers

Visible-Light-Mediated Organocatalyzed Thiol-Ene Reaction Initiated by a Proton-Coupled Electron Transfer

Levin, Vitalij V.,Dilman, Alexander D.

, p. 8337 - 8343 (2019/06/27)

A convenient method for performing a thiol-ene reaction is described. The reaction is performed under blue-light irradiation and catalyzed by photoactive Lewis basic molecules such as acridine orange or naphthalene-fused N-acylbenzimidazole. It is believed that the process is initiated by a proton-coupled electron transfer process within the complex between the thiol and the Lewis basic catalyst.

Aerial dioxygen activation: Vs. thiol-ene click reaction within a system

Choudhuri, Khokan,Mandal, Arkalekha,Mal, Prasenjit

supporting information, p. 3759 - 3762 (2018/04/16)

Markovnikov or anti-Markovnikov selective thiol-ene click (TEC) reactions and the synthesis of β-hydroxysulfides via aerial dioxygen activation are prevalent C-S bond forming reactions of styrenes and thiophenols. Herein, by choosing appropriate environme

Visible-Light-Promoted Remote C-H Functionalization of o-Diazoniaphenyl Alkyl Sulfones

Du, Shaofu,Kimball, Elizabeth Ann,Ragains, Justin R.

supporting information, p. 5553 - 5556 (2017/10/25)

Visible-light irradiation of ortho-diazoniaphenyl alkyl sulfones in the presence of Ru(bpy)32+ results in remote Csp3-H functionalization. Key mechanistic steps in these processes involve intramolecular hydrogen atom transfer from Csp3-H bonds to aryl radicals to generate alkyl/benzyl radicals. Subsequent polar crossover occurs by single-electron oxidation of the alkyl/benzyl radicals to carbenium ions that then intercept nucleophiles. We have developed remote hydroxylations, etherifications, an amidation, and C-C bond formation processes using this strategy.

Synthesis of aryl sulfides by decarboxylative C-S cross-couplings

Duan, Zhongyu,Ranjit, Sadananda,Zhang, Pengfei,Liu, Xiaogang

supporting information; experimental part, p. 3666 - 3669 (2009/12/07)

A study was conducted to demonstrate the transition-metal-catalyzed synthesis of aryl sulfides by decarboxylative C-S cross-couplings. Coupling reaction of 2-nitrobenzoic acid with 1-octanethiol were carried in the presence of different combinations of tr

Design and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors

Yang, Qingang,Chen, Lili,He, Xuchang,Gao, Zhenting,Shen, Xu,Bai, Donglu

scheme or table, p. 1400 - 1405 (2009/09/29)

The severe acute respiratory syndrome (SARS) coronavirus 3CL protease is an attractive target for the development of anti-SARS drugs. In this paper, cinanserin (1) analogs were synthesized and tested for the inhibitory activities against SARS-coronavirus (CoV) 3CL protease by fluorescence resonance energy transfer (FRET) assay. Four analogs show significant activities, especially compound 26 with an IC50 of 1.06 μM.

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