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Quinoline, 8-(methylsulfonyl)-, also known as 8-(methylsulfonyl)quinoline, is an organic compound with the chemical formula C10H10NO2S. It is a derivative of quinoline, a heterocyclic aromatic compound with a benzene ring fused to a pyridine ring. The 8-(methylsulfonyl) group is attached to the quinoline core, which introduces a methylsulfonyl functional group at the 8th position. Quinoline, 8-(methylsulfonyl)- is of interest in various chemical and pharmaceutical applications due to its unique structure and properties. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of new materials with specific properties. The compound is typically synthesized through various chemical reactions and can be characterized using techniques such as NMR and mass spectrometry.

5825-42-3

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5825-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5825-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5825-42:
(6*5)+(5*8)+(4*2)+(3*5)+(2*4)+(1*2)=103
103 % 10 = 3
So 5825-42-3 is a valid CAS Registry Number.

5825-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-methanesulfonyl-quinoline

1.2 Other means of identification

Product number -
Other names 8-Methansulfonyl-chinolin

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:5825-42-3 SDS

5825-42-3Downstream Products

5825-42-3Relevant academic research and scientific papers

High Chemoselectivity in the Construction of Aryl Methyl Sulfones via an Unexpected C-S Bond Formation between Sulfonylhydrazides and Dimethyl Phosphite

Liu, Teng,Yu, Shiwen,Shen, Xiang,Li, Yixian,Liu, Jianjun,Huang, Chao,Cheng, Feixiang

, p. 153 - 160 (2021/10/04)

A highly chemoselective route to aryl methyl sulfones via an unexpected C S bond formation between sulfonylhydrazides and dimethyl phosphite catalyzed by NaI under mild conditions has been established. This transformation provides an alternative and metal-free pathway to acquire various aryl methyl sulfones in good to excellent yields. Notably, dimethyl phosphite was employed as a stable and readily available alkyl source.

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