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1-chloro-2-(ethenylsulfonyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5535-44-4

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5535-44-4 Usage

Functional groups

Chlorine atom, Sulfonyl group, and Vinyl group

Structure

Chlorinated benzene derivative with a sulfonyl group attached to the second carbon atom

Applications

a. Intermediate in the synthesis of pharmaceuticals and agrochemicals
b. Production of dyes and pigments
c. Precursor in the manufacture of various organic compounds, including specialty chemicals and fine chemicals

Hazardous nature

Considered hazardous if not handled properly

Precautions

Safe handling and disposal measures should be taken to avoid exposure

Check Digit Verification of cas no

The CAS Registry Mumber 5535-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,3 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5535-44:
(6*5)+(5*5)+(4*3)+(3*5)+(2*4)+(1*4)=94
94 % 10 = 4
So 5535-44-4 is a valid CAS Registry Number.

5535-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-2-ethenylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names 1-chloro-2-ethenylsulfonyl-benzene

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:5535-44-4 SDS

5535-44-4Downstream Products

5535-44-4Relevant academic research and scientific papers

Metal-free visible-light-promoted C(sp3)-H functionalization of aliphatic cyclic ethers using trace O2

Blackburn, Bryan G.,Cooke, Maria Victoria,Laulhé, Sébastien,Niu, Ben,Sachidanandan, Krishnakumar

supporting information, p. 9454 - 9459 (2021/12/09)

Presented is a light-promoted C-C bond forming reaction yielding sulfone and phosphate derivatives at room temperature in the absence of metals or photoredox catalyst. This transformation proceeds in neat conditions through an auto-oxidation mechanism which is maintained through the leaching of trace amounts of O2 as sole green oxidant. This journal is

Bovine serum albumin-cobalt(II) Schiff base complex hybrid: An efficient artificial metalloenzyme for enantioselective sulfoxidation using hydrogen peroxide

Tang, Jie,Huang, Fuping,Wei, Yi,Bian, Hedong,Zhang, Wei,Liang, Hong

, p. 8061 - 8072 (2016/06/06)

An artificial metalloenzyme (BSA-CoL) based on the incorporation of a cobalt(ii) Schiff base complex {CoL, H2L = 2,2′-[(1,2-ethanediyl)bis(nitrilopropylidyne)]bisphenol} with bovine serum albumin (BSA) has been synthesized and characterized. Attention is focused on the catalytic activity of this artificial metalloenzyme for enantioselective oxidation of a variety of sulfides with H2O2. The influences of parameters such as pH, temperature, and the concentration of catalyst and oxidant on thioanisole as a model are investigated. Under optimum conditions, BSA-CoL as a hybrid biocatalyst is efficient for the enantioselective oxidation of a series of sulfides, producing the corresponding sulfoxides with excellent conversion (up to 100%), chemoselectivity (up to 100%) and good enantiomeric purity (up to 87% ee) in certain cases.

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