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p-Toluenesulfonic acid 2,4-dichlorophenyl ester is a chemical compound with the molecular formula C13H11Cl2O3S. It is an ester derivative of p-toluenesulfonic acid, where the hydroxyl group is replaced by a 2,4-dichlorophenyl group. p-Toluenesulfonic acid 2,4-dichlorophenyl ester is characterized by its white crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It is primarily used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. Due to its reactivity, it is essential to handle p-Toluenesulfonic acid 2,4-dichlorophenyl ester with care, following proper safety protocols to minimize potential health and environmental risks.

5328-03-0

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5328-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5328-03-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5328-03:
(6*5)+(5*3)+(4*2)+(3*8)+(2*0)+(1*3)=80
80 % 10 = 0
So 5328-03-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H10Cl2O3S/c1-9-2-5-11(6-3-9)19(16,17)18-13-7-4-10(14)8-12(13)15/h2-8H,1H3

5328-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-dichlorophenyl) 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names Toluol-4-sulfonsaeure-(2,4-dichlor-phenylester)

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:5328-03-0 SDS

5328-03-0Relevant articles and documents

Chromatography-Free and Eco-Friendly Synthesis of Aryl Tosylates and Mesylates

Lei, Xiangyang,Jalla, Anusha,Abou Shama, Mhd A.,Stafford, Jamie M.,Cao, Billy

supporting information, p. 2578 - 2585 (2015/09/01)

Two chromatography-free and eco-friendly protocols have been developed to synthesize aryl tosylates and mesylates by the tosylation and mesylation of the corresponding hydroxyarenes, respectively. These protocols are superior to other known ones regarding

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