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Ethyl 2,4,6-tri(propan-2-yl)benzenesulfonate is a complex organic chemical compound with the molecular formula C15H24O3S. It is a derivative of benzene, with three propyl groups (propan-2-yl) attached to the 2, 4, and 6 positions of the benzene ring, and an ethyl group attached to the sulfur atom of a sulfonate group. ethyl 2,4,6-tri(propan-2-yl)benzenesulfonate is characterized by its unique structure, which provides it with specific chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. Due to its complex structure, it is essential to handle ethyl 2,4,6-tri(propan-2-yl)benzenesulfonate with care and follow proper safety protocols during its synthesis and use.

7253-78-3

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7253-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7253-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7253-78:
(6*7)+(5*2)+(4*5)+(3*3)+(2*7)+(1*8)=103
103 % 10 = 3
So 7253-78-3 is a valid CAS Registry Number.

7253-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,4,6-tri(propan-2-yl)benzenesulfonate

1.2 Other means of identification

Product number -
Other names ethyl-2,4,6-tri-isopropylbenzenesulphonate

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:7253-78-3 SDS

7253-78-3Downstream Products

7253-78-3Relevant academic research and scientific papers

Selective Sulfonylating Agents

Guthrie, R. D. (Gus),Thang, San

, p. 2133 - 2136 (2007/10/02)

A variety of bulky sulfonyl chlorides have been investigated as sulfonylating reagents for polyol systems in an endeavour to find a selective reagent that would also give rise to a reactive sulfonate ester group.

Sulphone Formation from 2,4,6-Tri-isopropylbenzenesulphinic Acid

Adlington, Robert M.,Barrett, Anthony G. M.

, p. 1076 - 1079 (2007/10/02)

2,4,6-Tri-isopropylbenzenesulphinic acid decomposed in the presence of oxygen giving 2,4,6-tri-isopropyl-1,α-sultone; a mechanism involving arylsulphonyl and peroxyarylsulphonyl radicals and intramolecular hydrogen atom abstraction is suggested.

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