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116547-92-3

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116547-92-3 Usage

General Description

N-(2-Iodophenyl)methanesulfonamide, also known as IMS, is a chemical compound with the molecular formula C7H8INO2S. It is a sulfonamide derivative that contains an iodine atom and a phenyl group in its structure. IMS has been studied for its potential use as a reagent in organic synthesis and as a precursor for making pharmaceutical compounds. It has also been investigated for its antimicrobial and anti-inflammatory properties. Due to its unique structure and potential applications in various fields, N-(2-Iodophenyl)methanesulfonamide is a compound of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 116547-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,4 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116547-92:
(8*1)+(7*1)+(6*6)+(5*5)+(4*4)+(3*7)+(2*9)+(1*2)=133
133 % 10 = 3
So 116547-92-3 is a valid CAS Registry Number.

116547-92-3SDS

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 N-(2-iodophenyl)methanesulfonamide

1.2 Other means of identification

Product number -
Other names iodophenylmethanesulfonamide

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:116547-92-3 SDS

116547-92-3Relevant articles and documents

One-pot Sonogashira coupling, hydroamination of alkyne and intramolecular C–H arylation reactions toward the synthesis of indole-fused benzosultams

Debnath, Sudarshan,Mondal, Shovan

, p. 2260 - 2263 (2018)

A one-pot Sonogashira coupling, hydroamination of alkyne and C–H arylation reactions for the synthesis of indole-fused benzosultams are described. This method allows access to a variety of indole-fused seven membered benzosultams in good to excellent yiel

Oxidative Pictet-Spengler cyclisations through acceptorless iridium-catalysed dehydrogenation of tertiary amines

Cooksey, John P.,Saidi, Ourida,Williams, Jonathan M.J.,Blacker, A. John,Marsden, Stephen P.

supporting information, (2020/12/14)

The valuable tetrahydro-β- and γ-carboline skeleta can be accessed through Pictet-Spengler cyclisation initiated by acceptorless dehydrogenation of saturated cyclic amines. The substrate scope for the β-isomers is found to be somewhat limited, but access

Hydroarylation of Arenes via Reductive Radical-Polar Crossover

Flynn, Autumn R.,Mcdaniel, Kelly A.,Hughes, Meredith E.,Vogt, David B.,Jui, Nathan T.

supporting information, p. 9163 - 9168 (2020/07/10)

A photocatalytic system for the dearomative hydroarylation of benzene derivatives has been developed. Using a combination of an organic photoredox catalyst and an amine reductant, this process operates through a reductive radical-polar crossover mechanism where aryl halide reduction triggers a regioselective radical cyclization event, followed by anion formation and quenching to produce a range of complex spirocyclic cyclohexadienes. This light-driven protocol functions at room temperature in a green solvent system (aq. MeCN) without the need for precious metal-based catalysts or reagents or the generation of stoichiometric metal byproducts.

Iridium-Catalyzed Cycloisomerization of Alkynoic Acids: Synthesis of Unsaturated Lactones

Huang, Yi,Zhang, Xianghe,Dong, Xiu-Qin,Zhang, Xumu

supporting information, p. 782 - 788 (2020/01/08)

The iridium-catalyzed cycloisomerization of various alkynoic acids was successfully developed, and a series of five-, six-, and especially seven-membered unsaturated lactones were constructed with moderate yields and excellent regioselectivities (up to 68

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