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Ethyl 4-fluorobenzenesulfonate is an organic compound with the chemical formula C8H9FO3S. It is a colorless to pale yellow liquid that is soluble in organic solvents. ethyl 4-fluorobenzenesulfonate is a derivative of benzenesulfonate, featuring a fluorine atom at the para position relative to the sulfonate group. It is synthesized by reacting 4-fluorotoluene with chlorosulfonic acid, followed by the addition of ethanol. Ethyl 4-fluorobenzenesulfonate is used as an intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals due to its reactivity and the presence of the electron-withdrawing fluorine atom, which can influence the properties of the final products.

2924-72-3

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2924-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2924-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2924-72:
(6*2)+(5*9)+(4*2)+(3*4)+(2*7)+(1*2)=93
93 % 10 = 3
So 2924-72-3 is a valid CAS Registry Number.

2924-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluor-benzolsulfonsaeure-aethylester

1.2 Other means of identification

Product number -
Other names -

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

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More Details:2924-72-3 SDS

2924-72-3Downstream Products

2924-72-3Relevant academic research and scientific papers

Accelerated SuFEx Click Chemistry For Modular Synthesis**

Barrow, Andrew S.,Gialelis, Timothy L.,Homer, Joshua A.,Koelln, Rebecca A.,Moses, John E.,Smedley, Christopher J.

supporting information, (2021/12/10)

SuFEx click chemistry is a powerful method designed for the selective, rapid, and modular synthesis of functional molecules. Classical SuFEx reactions form stable S?O linkages upon exchange of S?F bonds with aryl silyl-ether substrates, and while near-per

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