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2297-65-6

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2297-65-6 Usage

General Description

Benzenesulfonyl bromide is a type of organosulfur compound with chemical formula C6H5SO2Br. It belongs to the class of organic compounds known as benzenesulfonyl compounds, which are chemical compounds containing a sulfur atom connected to a benzene ring via a sulfonyl group. It is used as an alkylating agent in organic synthesis, where it acts as a source of benzene-sulfonyl group (-SO2C6H5). It is a liquid that is highly corrosive and can cause burns and serious eye damage. It is sensitive to moisture and should be stored in a dry place.

Check Digit Verification of cas no

The CAS Registry Mumber 2297-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,9 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2297-65:
(6*2)+(5*2)+(4*9)+(3*7)+(2*6)+(1*5)=96
96 % 10 = 6
So 2297-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrO2S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H

2297-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzenesulfonyl bromide

1.2 Other means of identification

Product number -
Other names Benzolsulfobromid

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:2297-65-6 SDS

2297-65-6Relevant articles and documents

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Cristol,S.J. et al.

, p. 1529 - 1532 (1966)

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Synergistic Dual Role of [hmim]Br-ArSO2Cl in Cascade Sulfenylation-Halogenation of Indole: Mechanistic Insight into Regioselective C-S and C-S/C-X (X = Cl and Br) Bond Formation in One Pot

Equbal, Danish,Singh, Richa,Saima,Lavekar, Aditya G.,Sinha, Arun K.

supporting information, p. 2660 - 2675 (2019/03/14)

Bifunctionalized indoles are an important class of biologically active heterocyclic compounds and potential drug candidates. Because of the lack of efficient synthetic methods, one pot cascade synthesis of these compounds is rare and remains a challenge.

Sulfonyl halide synthesis by thiol oxyhalogenation using NBS/NCS – iPrOH

Silva-Cuevas, Carolina,Perez-Arrieta, Carlos,Polindara-García, Luis A.,Lujan-Montelongo, J. Armando

supporting information, p. 2244 - 2247 (2017/05/16)

A rapid and facile method provides a general route to sulfonyl bromides/chlorides by the oxidation of thiols using NXS – ROH (X?=?Br,Cl, R?=?iPr) as an oxyhalogenation reagent. Control experiments suggest that the alcohol component is the source of oxygen. The proposed method enable the access to structurally diverse sulfonyl bromides and chlorides including challenging examples, inaccessible by other synthetic methods.

METHOD FOR PRODUCING SULFONYL BROMIDE COMPOUNDS

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Paragraph 0032, (2017/04/27)

PROBLEM TO BE SOLVED: To provide a method capable of producing sulfonyl bromide compounds which are useful as an intermediate such as a medicine, an agrochemical and a functional materials safely, simply and in a high yield. SOLUTION: There is provided a

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