1669-36-9

Basic information

• Product Name: 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methyl-
• CAS NO: 1669-36-9
• Molecular Formula: C15H23BrO
• Molecular Weight: 299.251
• Mol File: 1669-36-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methyl-(1669-36-9)
• EPA Substance Registry System: 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methyl-(1669-36-9)

Safety Data

• Hazardous Substances Data: 1669-36-9(Hazardous Substances Data)

Usage

General Description

2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methyl- is a chemical compound with the molecular formula C15H21BrO. It is a yellowish-brown liquid that is insoluble in water. 2,5-Cyclohexadien-1-one, 4-bromo-2,6-bis(1,1-dimethylethyl)-4-methyl- is commonly used as a synthetic intermediate in the production of pharmaceuticals and agrochemicals. It is also used in the manufacturing of fragrances and flavors. Additionally, it has been studied for its potential antifungal and antimicrobial properties. However, it is important to handle this compound with caution and use appropriate safety measures, as it is flammable and may cause skin and eye irritation.

Upstream product

• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 10218-83-4 N,N-dibromomethylamine 

Downstream Products

• 2091-51-2 4-(bromomethyl)-2,6-di-tert-butylphenol 
• 1516-94-5 1,2-bis(3,5-di-tert-butyl-4-hydroxyphenyl)ethane 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 809-73-4 3,3',5,5'-tetra-tert-butyl-4,4'-stilbenequinone 
• 10396-80-2 2,6-di-tert-butyl-4-hydroxy-4-methylcyclohexa-2,5-dienone 
• 38876-35-6 2,6-di-tert-butyl-4-ethoxy-4-methylcyclohexa-2,5-dienone 
• 1219595-77-3 2,6-di-tert-butyl-4-isopropoxy-4-methylcyclohexa-2,5-dienone 
• 89687-11-6 3,5-di-tert-butyl-4-hydroxybenzyl tert-butyl ether 
• 89687-10-5 2,6-di-tert-butyl-4-tert-butoxy-4-methylcyclohexa-2,5-dienone 
• 1620-98-0 3,5-di-t-butyl-4-hydroxybenzaldehyde 
• 98195-65-4 α,α'-dibromo-3,5,3',5'-tetra-tert-butyl-bibenzyl-4,4'-diol 
• 97084-66-7 3,5,3',5'-tetra-tert-butyl-α,α'-dichloro-bibenzyl-4,4'-diol 
• 88-26-6 3,5-di-tert-butyl-4-hydroxybenzyl alcohol 
• 2950-01-8 2,6-di-tert-butyl-4-[(E)-2-(3,5-di-tert-butyl-4-hydroxyphenyl)ethenyl]phenol 

Relevant articles and documents

Oxidation Using Quaternary Ammonium Polyhalides. IX. Oxidation of Hindered Phenols with Benzyltrimethylammonium Tribromide

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.