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"(difluoromethyl)(m-tolyl)sulfane" is a chemical compound with the formula C8H8F2S. It is a derivative of sulfane, where a difluoromethyl group (-CF2H) and a m-tolyl group (-C6H4CH3, with the methyl group at the meta position) are attached to the sulfur atom. (difluoromethyl)(m-tolyl)sulfane is an example of an organosulfur compound, which can be used in various chemical reactions and applications, such as in the synthesis of pharmaceuticals or as a reagent in organic chemistry. The presence of the difluoromethyl group may impart unique properties to the molecule, such as increased lipophilicity or altered reactivity, depending on the context of its use.

4837-10-9

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4837-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4837-10-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4837-10:
(6*4)+(5*8)+(4*3)+(3*7)+(2*1)+(1*0)=99
99 % 10 = 9
So 4837-10-9 is a valid CAS Registry Number.

4837-10-9Relevant academic research and scientific papers

Visible light-promoted difluoromethylthiolation of aryldiazonium salts

Wang, Wengui,Zhang, Shuxiang,Zhao, Huaiqing,Wang, Shoufeng

, p. 8565 - 8568 (2018/11/27)

Difluoromethylthiolation of aryldiazonium salts under photocatalytic conditions with a shelf-stable, easily prepared and inexpensive reagent, PhSO2SCF2H was described. A variety of difluoromethylthioethers were obtained utilizing aryldiazonium salts containing different functional groups. Aryldiazonium salts with a heteroarene moiety were tolerated. Fluorescence quenching experiments indicated that both oxidative and reductive quenching cycles occurred during this process.

Visible-Light Photoredox Difluoromethylation of Phenols and Thiophenols with Commercially Available Difluorobromoacetic Acid

Yang, Jinyan,Jiang, Min,Jin, Yunhe,Yang, Haijun,Fu, Hua

supporting information, p. 2758 - 2761 (2017/05/24)

A simple and efficient visible-light photoredox one-pot method for difluoromethylation of phenols and thiophenols has been developed. The protocol uses commercially available, inexpensive, and easy handling difluorobromoacetic acid as the difluoromethylating agent, and the diverse O- and S-difluoromethylated products were prepared in good yields with tolerance of many functional groups.

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