13836-48-1 Usage
Uses
Used in Epoxy Resin Production:
Bisphenol A (3-chloro-2-hydroxypropyl) G is used as a crosslinking agent in the production of epoxy resins, providing improved strength and durability to the final product. Its ability to form strong chemical bonds with other components in the resin system contributes to the enhanced mechanical properties of the resulting materials.
Used in Polycarbonate Plastics:
This chemical compound is also utilized in the production of polycarbonate plastics, which are known for their high impact resistance, transparency, and heat resistance. Bisphenol A (3-chloro-2-hydroxypropyl) G plays a crucial role in the polymerization process, contributing to the formation of the polycarbonate structure.
Used in Flame Retardant Synthesis:
Bisphenol A (3-chloro-2-hydroxypropyl) G is employed as a raw material in the synthesis of flame retardants, which are essential in various industries to improve the fire safety of materials. Its high thermal stability and electrical insulating properties make it a valuable component in the development of effective flame retardants.
Used in Coatings and Adhesives:
In the coatings and adhesives industry, Bisphenol A (3-chloro-2-hydroxypropyl) G is used to improve the adhesion, flexibility, and durability of the final products. Its crosslinking properties contribute to the formation of strong bonds between the coating or adhesive and the substrate, resulting in enhanced performance.
Used in Electrical and Electronic Applications:
Due to its electrical insulating properties, Bisphenol A (3-chloro-2-hydroxypropyl) G is used in the manufacturing of electrical and electronic components, such as insulating materials for transformers, capacitors, and circuit boards. Its high thermal stability ensures the reliability and longevity of these components in various applications.
However, it is important to note that the use of Bisphenol A (3-chloro-2-hydroxypropyl) G has been subject to regulations and restrictions in certain applications due to its potential health risks, including endocrine disruption and reproductive toxicity. As a result, industries are continuously exploring alternative materials and methods to minimize the use of this chemical compound while maintaining the desired properties and performance of their products.
Check Digit Verification of cas no
The CAS Registry Mumber 13836-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,3 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13836-48:
(7*1)+(6*3)+(5*8)+(4*3)+(3*6)+(2*4)+(1*8)=111
111 % 10 = 1
So 13836-48-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H25ClO4/c1-21(2,15-3-7-18(8-4-15)24-12-17(23)11-22)16-5-9-19(10-6-16)25-13-20-14-26-20/h3-10,17,20,23H,11-14H2,1-2H3
13836-48-1Relevant academic research and scientific papers
BISPHENOL COMPOUNDS AND METHODS FOR THEIR USE
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Page/Page column 88, (2012/10/18)
Compounds having a structure of Formula I: wherein G, a, Q, L2, R1, R2, R3, R4, R5 and R6 are as defined herein are provided. Uses of such compounds for treatment of various indications, including prostate cancer as well as methods of treatment involving such compounds are also provided.
Process for manufacturing an alpha-dihydroxy derivative and epoxy resins prepared therefrom
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Page/Page column 41-42, (2008/06/13)
A process for manufacturing an α-dihydroxy derivative from an aryl allyl ether wherein such α-dihydroxy derivative can be used to prepare an α-halohydrin intermediate and an epoxy resin prepared therefrom including epoxidizing an α-halohydrin intermediate produced from a halide substitution of an α-dihydroxy derivative which has been obtained by a dihydroxylation reaction of an aryl allyl ether in the presence of an oxidant or in the presence of an oxidant and a catalyst.
