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(E)-(2-oxodihydrofuran-3(2H)-ylidene)methyl 4-methylbenzenesulfonate is a chemical compound characterized by its molecular formula C13H12O5S. It is a sulfonate ester derivative of 4-methylbenzenesulfonic acid, featuring a dihydrofuran ring. (E)-(2-oxodihydrofuran-3(2H)-ylidene)methyl 4-methylbenzenesulfonate is recognized for its unique properties and versatility in chemical transformations, making it a valuable asset in various applications.

76299-53-1

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76299-53-1 Usage

Uses

Used in Organic Synthesis:
(E)-(2-oxodihydrofuran-3(2H)-ylidene)methyl 4-methylbenzenesulfonate is used as a reagent in organic synthesis for its ability to participate in various chemical reactions. Its capacity to form carbon-carbon and carbon-heteroatom bonds makes it a useful component in creating complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E)-(2-oxodihydrofuran-3(2H)-ylidene)methyl 4-methylbenzenesulfonate serves as a key compound for the synthesis of potential drug molecules. Its unique chemical properties allow for the development of new therapeutic agents with diverse mechanisms of action.
Used as a Building Block in Pharmaceutical Intermediates and Fine Chemicals:
(E)-(2-oxodihydrofuran-3(2H)-ylidene)methyl 4-methylbenzenesulfonate is also utilized as a building block in the preparation of pharmaceutical intermediates and fine chemicals. Its incorporation into these compounds can enhance their efficacy, stability, or other desirable attributes, contributing to the advancement of pharmaceutical research and development.
Overall, (E)-(2-oxodihydrofuran-3(2H)-ylidene)methyl 4-methylbenzenesulfonate is an important compound in numerous chemical applications due to its unique properties and its role in the synthesis of various molecules with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 76299-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,9 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76299-53:
(7*7)+(6*6)+(5*2)+(4*9)+(3*9)+(2*5)+(1*3)=171
171 % 10 = 1
So 76299-53-1 is a valid CAS Registry Number.

76299-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-(2-oxooxolan-3-ylidene)methyl] 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 3-(toluene-4-sulfonyloxymethylene)-dihydro-furan-2-one

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:76299-53-1 SDS

76299-53-1Relevant academic research and scientific papers

Allergenic α-Methylene-γ-lactones. General Method for the Preparation of β-Acetoxy- and β-Hydroxy-α-methylene-γ-butyrolactones from Sulfoxides. Application to the Synthesis of a Tuliposide B Derivative

Corbet, Jean-Pierre,Benezra Claude

, p. 1141 - 1147 (2007/10/02)

A general synthesis of β-hydroxy-α-methylene-γ-butyrolactones , which is based on the sulfoxide-sulfenate rearrangement, is presented.Several β-acetoxy-α-methylene-γ-butyrolactones have been prepared and transformed into the β-hydroxy-derivatives through base hydrolysis.This synthesis has been applied to the first preparation of (tetraacetoxybenzyl)tuliposide B (22).

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