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3,5,3',5'-Tetramethyl-4,4'-methanediyl-di-phenol, also known as bisphenol A (BPA), is an organic compound with the chemical formula C15H16O2. It is a white crystalline solid that is widely used in the production of polycarbonate plastics and epoxy resins. BPA is found in various consumer products, including food and beverage containers, dental sealants, and thermal receipt paper. It has been a subject of concern due to its potential endocrine-disrupting properties and health risks associated with long-term exposure. Studies have shown that BPA can leach into food and beverages from containers, raising concerns about its impact on human health, particularly in relation to reproductive and developmental issues. As a result, many countries have restricted or banned the use of BPA in certain products, and alternative materials are being developed to replace it in various applications.

3692-14-6

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3692-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3692-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3692-14:
(6*3)+(5*6)+(4*9)+(3*2)+(2*1)+(1*4)=96
96 % 10 = 6
So 3692-14-6 is a valid CAS Registry Number.

3692-14-6Downstream Products

3692-14-6Relevant academic research and scientific papers

Silica Gel as an Effective Catalyst for the Alkylation of Phenols and Some Heterocyclic Compounds

Kamitori, Yasuhiro,Hojo, Masaru,Masuda, Ryoichi,Izumi, Tatsuo,Tsukamoto, Shuichi

, p. 4161 - 4165 (2007/10/02)

In the presence of silica gel, the reaction of phenol with t-BuBr was examined under a variety of conditions and it was found that silica gel is an effective catalyst for the alkylation.As a result of this work 2-tert-butyl-, 2,6-di-tert-butyl-, and 2,4,6-tri-tert-butylphenols, all of which are hard to obtain directly by the Friedel-Crafts process, could be prepared easily by this one-step reaction.Several other alkyl halides were also used in this reaction.The alkylations of some heterocyclic aromatic compounds which cannot be alkylated by the conventional Friedel-Crafts method were also succesfully performed by this reaction.

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