16002-30-5 Usage
Uses
Used in Polymer Production:
Acetic acid, 2,2'-sulfonylbis-, 1,1'-dimethyl ester is used as a crosslinking agent in the polymer industry for its ability to improve the structural properties and durability of the final products. It is commonly used in the synthesis of plastics, adhesives, and other industrial materials.
Used in Chemical Processes as a Solvent:
In addition to its role in polymer production, Acetic acid, 2,2'-sulfonylbis-, 1,1'-dimethyl ester is also employed as a solvent in some chemical processes, where its reactivity and properties are beneficial for specific applications.
Safety Precautions:
It is important to handle Acetic acid, 2,2'-sulfonylbis-, 1,1'-dimethyl ester with caution, as it can be irritating to the skin and eyes, and can cause respiratory issues if inhaled in high concentrations. Proper safety measures should be taken during its use to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 16002-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,0 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16002-30:
(7*1)+(6*6)+(5*0)+(4*0)+(3*2)+(2*3)+(1*0)=55
55 % 10 = 5
So 16002-30-5 is a valid CAS Registry Number.
16002-30-5Relevant academic research and scientific papers
1,4-Pentadien-3-ones, 25. - Reactions of 1,5-Diaryl-3-thia-1,4-pentadiene Derivatives with Substituted Hydroxylamines
Kleffel, Dagmar,Kratky, Christoph,Otto, Hans-Hartwig
, p. 1012 - 1020 (2007/10/02)
4-Methoxy-1,4-thiazinanes 6 are obtained by methylation of the parent 4-hydroxy compounds 2, but not by reaction of the title compounds 1 with O-methylhydroxylamine.However, when 1 reacts with N-methylhydroxylamine the 4-methylthiazinanes 10 are obtained.A reaction pathway for their formation is proposed.From the α,α'-disubstituted 3-thiapentadiene derivatives 3-5 only 4 reacts with N-methylhydroxylamine to yield 14.The structure of 10a is established by an X-ray analysis.
