1669-36-9 Usage
Uses
Used in Pharmaceutical Industry:
2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methylis used as a synthetic intermediate for the production of pharmaceuticals. Its unique chemical structure allows it to be a key component in the synthesis of various drugs, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methylis utilized as a synthetic intermediate for the creation of agrochemicals. Its properties make it suitable for use in the development of pesticides and other agricultural chemicals, helping to improve crop yields and protect plants from pests.
Used in Fragrance and Flavor Industry:
2,5-Cyclohadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methylis also used in the manufacturing of fragrances and flavors. Its unique chemical composition contributes to the creation of various scents and tastes, enhancing the sensory experience of consumer products.
Used in Antifungal and Antimicrobial Applications:
Research has shown that 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methylhas potential antifungal and antimicrobial properties. It is being studied for its ability to inhibit the growth of certain fungi and bacteria, which could lead to its use in various applications, such as in the development of disinfectants and preservatives.
It is important to handle 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methylwith caution and use appropriate safety measures, as it is flammable and may cause skin and eye irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 1669-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1669-36:
(6*1)+(5*6)+(4*6)+(3*9)+(2*3)+(1*6)=99
99 % 10 = 9
So 1669-36-9 is a valid CAS Registry Number.
1669-36-9Relevant academic research and scientific papers
Oxidation Using Quaternary Ammonium Polyhalides. IX. Oxidation of Hindered Phenols with Benzyltrimethylammonium Tribromide
Kajigaeshi, Shoji,Morikawa, Yukihiro,Fujisaki, Shizuo,Kakinami, Takaaki,Nishihira, Keigo
, p. 1060 - 1062 (2007/10/02)
Reactions of hindered phenols, such as 2,6-di-t-butyl-4-methylphenol, 3,5-di-t-butyl-4-hydroxybenzyl alcohol, and 2,6-di-t-butylphenol, with benzyltrimethylammonium tribromide were carried out in dichloromethane in the presence of water, t-butyl alcohol, or aqueous sodium hydroxide at room temperature.Sequential reaction processes were provided by the obtained products.
