14569-76-7 Usage
Uses
Used in Pharmaceutical Industry:
But-2-ynylene bis(chloroacetate) is used as a chemical intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, But-2-ynylene bis(chloroacetate) serves as a precursor in the production of various agrochemicals, aiding in the creation of effective pest control and crop protection solutions.
Used in Dye Industry:
But-2-ynylene bis(chloroacetate) is utilized as a chemical intermediate in the synthesis of dyes, playing a role in the development of colorants for textiles, plastics, and other materials.
Used in Polymer Production:
But-2-ynylene bis(chloroacetate) is employed in the production of polymers, where it contributes to the formation of polymeric materials with specific properties for various applications.
Used in Coatings and Adhesives Industry:
It is used as a component in the formulation of coatings and adhesives, enhancing their performance characteristics such as adhesion, durability, and resistance to environmental factors.
However, it is crucial to handle But-2-ynylene bis(chloroacetate) with care due to its potential harmful effects if inhaled or ingested, and its ability to cause skin and eye irritation. Proper safety measures should be taken during its use to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 14569-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,6 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14569-76:
(7*1)+(6*4)+(5*5)+(4*6)+(3*9)+(2*7)+(1*6)=127
127 % 10 = 7
So 14569-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2O4/c9-5-7(11)13-3-1-2-4-14-8(12)6-10/h3-6H2
14569-76-7Relevant academic research and scientific papers
Synthesis of new AB2 monomers for polymerization to hyperbranched polymers by 1,3-dipolar cycloaddition
Smet, Mario,Metten, Kris,Dehaen, Wim
, p. 1097 - 1108 (2007/10/03)
A number of AB2 monomers containing either one azide and two acetylene functions or vice versa have been prepared. Upon polymerization, these compounds were found to give rise to hyperbranched oligomers as detected by NMR spectroscopy. However, the formation of high-molecular-weight polymers could not be proven by GPC analysis. Crosslinking was found to be a major drawback of this approach to hyperbranched polymers. Two examples of the interesting situation in which the polymerization already starts during the introduction of the polymerizable group are described.
