53333-76-9 Usage
Uses
Used in Organic Synthesis:
2,2-DIMETHYLPROPANE-1-SULFONYL CHLORIDE is used as a reagent for introducing sulfonyl groups into organic molecules, which is crucial for the synthesis of various chemical compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,2-DIMETHYLPROPANE-1-SULFONYL CHLORIDE is used as a building block for chemical reactions that lead to the development of new drugs.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 2,2-DIMETHYLPROPANE-1-SULFONYL CHLORIDE is utilized as a key intermediate in the synthesis of various agrochemicals, contributing to the development of effective crop protection products.
Used in Industrial and Specialty Chemicals Synthesis:
2,2-DIMETHYLPROPANE-1-SULFONYL CHLORIDE is also employed as an intermediate in the synthesis of a wide range of industrial and specialty chemicals, highlighting its importance in the chemical industry.
Safety Precautions:
Due to its potent reactivity and potential hazards, it is essential to follow proper safety precautions when handling and using 2,2-DIMETHYLPROPANE-1-SULFONYL CHLORIDE to ensure the safety of personnel and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 53333-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,3 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53333-76:
(7*5)+(6*3)+(5*3)+(4*3)+(3*3)+(2*7)+(1*6)=109
109 % 10 = 9
So 53333-76-9 is a valid CAS Registry Number.
53333-76-9Relevant academic research and scientific papers
Novel, selective indole-based ECE inhibitors: Lead optimization via solid-phase and classical synthesis
Brands, Michael,Ergueden, Jens-Kerim,Hashimoto, Kentaro,Heimbach, Dirk,Schroeder, Christian,Siegel, Stephan,Stasch, Johannes-Peter,Weigand, Stefan
, p. 4201 - 4205 (2007/10/03)
A novel class of indole-based endothelin-converting enzyme (ECE) inhibitors was identified by high throughput screening. We report systematic optimization of this compound class by means of classical and solid-phase chemistry. Optimized compounds with a bisarylamide side chain at the 2-position of the indole skeleton exhibit low-nanomolar activity on ECE.
