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4-methylquinolin-2-yl 4-methylbenzenesulfonate is a complex organic chemical compound characterized by a quinoline ring structure with a methyl group at the 4-position and a 4-methylbenzenesulfonate group attached to it. 4-methylquinolin-2-yl 4-methylbenzenesulfonate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure. The 4-methylbenzenesulfonate group provides a sulfonyl moiety, which can be a key functional group in many chemical reactions, while the quinoline ring is a common structural motif in a variety of biologically active molecules. The combination of these features makes 4-methylquinolin-2-yl 4-methylbenzenesulfonate an interesting starting material for the development of new compounds with specific properties and applications in the fields of medicine and chemistry.

5465-88-3

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5465-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5465-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5465-88:
(6*5)+(5*4)+(4*6)+(3*5)+(2*8)+(1*8)=113
113 % 10 = 3
So 5465-88-3 is a valid CAS Registry Number.

5465-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylquinolin-2-yl) 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 2-tosyloxylepidine

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:5465-88-3 SDS

5465-88-3Relevant academic research and scientific papers

Catalyst-Controlled Selectivity in the Synthesis of C2- and C3-Sulfonate Esters from Quinoline N-Oxides and Aryl Sulfonyl Chlorides

Ying, Beibei,Xu, Jun,Zhu, Xiaolei,Shen, Chao,Zhang, Pengfei

, p. 2604 - 2608 (2016/08/30)

The first example of the catalyst-controlled selective synthesis of C2- and C3-sulfonate-ester-substituted quinolines was developed by employing LaCl3 and chitosan@CuI catalysts, respectively. This protocol provides an expeditious route to an important class of quinoline derivatives frequently found in many biologically active compounds and features good practicality, high efficiency, and environmental friendliness. In addition, the easily recoverable chitosan@copper catalysts can be recycled five times without significant loss of catalytic performance.

Pd-catalyzed direct cross-coupling of electron-deficient polyfluoroarenes with heteroaromatic tosylates

Fan, Shilu,Yang, Jie,Zhang, Xingang

supporting information; experimental part, p. 4374 - 4377 (2011/10/08)

We report a Pd-catalyzed direct cross-coupling of electron-deficient polyfluoroarenes with heteroaromatic tosylates. The notable features of this reaction are its high reaction efficiency, excellent chemoselectivity, operational simplicity, and mild react

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