2225-23-2 Usage
Uses
Used in Polymer Chemistry:
Ethylene Di(thiotosylate) is used as a linking or cross-linking agent for enhancing the properties of polymers, such as their strength, flexibility, and durability. Its reactivity allows for the formation of new bonds and connections between polymer chains, leading to improved material characteristics.
Used in Industrial Chemicals:
In the field of industrial chemicals, Ethylene Di(thiotosylate) is used as a key component in the synthesis of new materials and substances. Its role in creating novel compounds and products is instrumental in advancing various industries, from manufacturing to pharmaceuticals.
Used in Material Science:
Ethylene Di(thiotosylate) is employed in material science research and development, where its reactivity and ability to form cross-links contribute to the creation of innovative materials with unique properties. These materials can be tailored for specific applications, such as high-performance plastics or advanced composites.
Check Digit Verification of cas no
The CAS Registry Mumber 2225-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2225-23:
(6*2)+(5*2)+(4*2)+(3*5)+(2*2)+(1*3)=52
52 % 10 = 2
So 2225-23-2 is a valid CAS Registry Number.
2225-23-2Relevant academic research and scientific papers
A convenient one-pot preparation of stable equivalents of cyclobutane-1,2-dione and cyclobutanetrione
Deguest, Geoffrey,Bischoff, Laurent,Fruit, Corinne,Marsais, Francis
, p. 841 - 847 (2008/09/17)
A very short, high-yielding, one-pot procedure has been developed for the preparation of half-protected cyclobutane-1,2-dione. This compound is much more stable than cyclobutane-1,2-dione itself and allowed further transformation to give diprotected cyclobutanetrione equivalents. Copyright Taylor & Francis Group, LLC.
Preparation and Thermal Properties of N-Alkylidene-ethenesulfenamides
Ruel, Odile,Baudin, Jean-Bernard,Julia, Sylvestre A.
, p. 2151 - 2164 (2007/10/02)
A convenient preparation of N,N-bis(trimethylsilyl)-ethenesulfenamides is described, together with its fluoride-catalysed reaction with aldehydes or ketones to provide several N-alkylidene-ethenesulfenamides.On mild heating, two of these S-vinyl-thio-oximes can converted into the corresponding substituted pyrroles.
