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657-46-5

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657-46-5 Usage

General Description

1-Fluoro-3-(methylsulfonyl)benzene is a chemical compound with the molecular formula C7H7FO2S. It is also known by the trade name Deoxysugen. 1-Fluoro-3-(methylsulfonyl)benzene is a fluoroalkylsulfonylbenzene and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is known for its use in the production of anti-inflammatory drugs and is also used in the manufacturing of dyes and pigments. 1-Fluoro-3-(methylsulfonyl)benzene is a flammable liquid that should be handled with care due to its potential hazards if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 657-46-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 657-46:
(5*6)+(4*5)+(3*7)+(2*4)+(1*6)=85
85 % 10 = 5
So 657-46-5 is a valid CAS Registry Number.

657-46-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-3-methylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names 3-Fluorophenyl methyl sulfone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:657-46-5 SDS

657-46-5Relevant articles and documents

Switchable Synthesis of Aryl Sulfones and Sulfoxides through Solvent-Promoted Oxidation of Sulfides with O2/Air

Cheng, Zhen,Sun, Pengchao,Tang, Ailing,Jin, Weiwei,Liu, Chenjiang

supporting information, p. 8925 - 8929 (2019/11/14)

A practical and switchable method for the synthesis of aryl sulfones and sulfoxides via sulfide oxidation was developed. The chemoselectivities of products were simply controlled by reaction temperature using O2/air as the terminal oxidant and oxygen source. The broad substrate scope, easy realization of gram-scale production, and the simplification of a sulfide oxidation system render the strategy attractive and valuable.

Dynamics of cetyltrimethylammonium bromide-mediated reaction of phenylsulfinylacetic acid with Cr(VI): Treatment of pseudo-phase models

Subramaniam, Perumal,Selvi, Natesan Thamil

, p. 1019 - 1034 (2015/11/27)

The influence of cetyltrimethylammonium bromide, CTAB, on the oxidative decarboxylation of phenylsulfinylacetic acid, PSAA, and several meta- and para-substituted PSAAs by Cr(VI) was investigated in 95 % H2O-5 % CH3CN medium. The rate profile displayed a peculiar trend with an initial rate increase at low CTAB followed by sharp rate inhibition at higher CTAB concentrations. The initial rate acceleration could be explained by strong binding of SO42- on the positively charged micellar surface. The specific partitioning of PSAA in the micellar phase by hydrophobic interaction and the oxidizing species HCrO3+ in aqueous phase by electrostatic repulsion accounted for the rate retardation at higher CTAB concentrations. The Hammett plot with different substituted PSAAs showed excellent correlation affording negative ? value, which supports the proposed mechanism involving the intermediate formation of sulfonium cation. The obtained ? value in CTAB medium was found to be slightly lower than that in aqueous medium. Quantitative analysis of the rate data for the inhibition shown by CTAB was performed using the Menger-Portnoy and the Piszkiewicz pseudo-phase models. The binding constant for PSAA with micelles was evaluated from the Piszkiewicz cooperative model.

Copper-catalyzed aerobic oxidation and cleavage/formation of C-S bond: A novel synthesis of aryl methyl sulfones from aryl halides and DMSO

Yuan, Gaoqing,Zheng, Junhua,Gao, Xiaofang,Li, Xianwei,Huang, Liangbin,Chen, Huoji,Jiang, Huanfeng

supporting information; experimental part, p. 7513 - 7515 (2012/10/07)

With atmospheric oxygen as the oxidant, a novel copper(i)-catalyzed synthesis of aryl methyl sulfones from aryl halides and widely available DMSO is described. The procedure tolerates aryl halides with various functional groups (such as methoxy, acetyl, chloro, fluoro and nitro groups), which could afford aryl methyl sulfones in moderate to high yields. The copper-catalyzed aerobic oxidation and the cleavage/formation of C-S bond are the key steps for this transformation.

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