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2,3,4,5,6-PENTAFLUOROPHENYL 1-ETHANESULFONATE, with the chemical formula C8H5F5O3S, is a sulfonate ester that features a pentafluorophenyl group and an ethane linker. 2,3,4,5,6-PENTAFLUOROPHENYL 1-ETHANESULFONATE is recognized for its role as a reagent in organic synthesis, where it functions as a leaving group in a variety of chemical reactions. Its capacity to promote nucleophilic substitution reactions has made it a valuable component in the synthesis of pharmaceuticals and agrochemicals. Furthermore, its potential applications extend to the fields of materials science and polymer chemistry, where it is being explored for its unique properties and reactivity.

597553-60-1

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597553-60-1 Usage

Uses

Used in Organic Synthesis:
2,3,4,5,6-PENTAFLUOROPHENYL 1-ETHANESULFONATE is used as a reagent for facilitating nucleophilic substitution reactions in organic synthesis. Its structure allows it to act as an effective leaving group, which is crucial for the successful completion of many organic reactions.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2,3,4,5,6-PENTAFLUOROPHENYL 1-ETHANESULFONATE is utilized as a key intermediate in the synthesis of various drugs. Its ability to participate in nucleophilic substitution reactions aids in the creation of complex molecular structures required for medicinal compounds.
Used in Agrochemical Synthesis:
Similarly, in agrochemical synthesis, 2,3,4,5,6-PENTAFLUOROPHENYL 1-ETHANESULFONATE serves as an essential reagent, contributing to the development of new pesticides and other agricultural chemicals through its role in nucleophilic substitution reactions.
Used in Materials Science:
2,3,4,5,6-PENTAFLUOROPHENYL 1-ETHANESULFONATE is also used in materials science as a component in the development of new materials. Its unique properties and reactivity make it a candidate for creating advanced materials with specific characteristics.
Used in Polymer Chemistry:
In the field of polymer chemistry, 2,3,4,5,6-PENTAFLUOROPHENYL 1-ETHANESULFONATE is employed in the synthesis of polymers with tailored properties. Its role in facilitating reactions allows for the creation of polymers with specific functionalities and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 597553-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,7,5,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 597553-60:
(8*5)+(7*9)+(6*7)+(5*5)+(4*5)+(3*3)+(2*6)+(1*0)=211
211 % 10 = 1
So 597553-60-1 is a valid CAS Registry Number.

597553-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentafluorophenyl) ethanesulfonate

1.2 Other means of identification

Product number -
Other names Ethanesulfonic acid,pentafluorophenyl ester

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:597553-60-1 SDS

597553-60-1Upstream product

597553-60-1Downstream Products

597553-60-1Relevant academic research and scientific papers

Direct Synthesis of Sulfonamides and Activated Sulfonate Esters from Sulfonic Acids

Caddick, Stephen,Wilden, Jonathan D.,Judd, Duncan B.

, p. 1024 - 1025 (2007/10/03)

A general new method for the preparation of sulfonamides and activated sulfonate esters by the direct coupling of sulfonic acid salts with amines and alcohols using the reagent triphenylphosphine ditriflate is described. A new reusable polymer-supported reagent for these transformations under heterogeneous conditions is also described. These methods provide a fundamentally new approach to making small molecules containing the sulfonamide functional group. Copyright

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