125237-08-3

Basic information

• Product Name: 2-BroMo-3,5-diMethylphenol
• Synonyms: 2-BroMo-3,5-diMethylphenol
• CAS NO: 125237-08-3
• Molecular Formula: C₈H₉BrO
• Molecular Weight: 201.06046
• Mol File: 125237-08-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-BroMo-3,5-diMethylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BroMo-3,5-diMethylphenol(125237-08-3)
• EPA Substance Registry System: 2-BroMo-3,5-diMethylphenol(125237-08-3)

Safety Data

• Hazardous Substances Data: 125237-08-3(Hazardous Substances Data)

Usage

General Description

2-Bromo-3,5-dimethylphenol is a chemical compound with the formula C8H9BrO. It is a derivative of phenol with two methyl groups and a bromine atom attached to the benzene ring. This chemical is commonly used as a disinfectant and antiseptic due to its antimicrobial properties. It is also utilized in the synthesis of pharmaceuticals and as an intermediate in organic synthesis. Additionally, 2-Bromo-3,5-dimethylphenol has been studied for its potential use in various medical and industrial applications, including in the treatment of bacterial infections and as a preservative in personal care products. However, it is important to handle this compound with care, as it is considered hazardous if ingested, inhaled, or comes into contact with the skin.

Upstream product

• 108-68-9 3,5-Dimethylphenol 

Relevant articles and documents

Trifluoromethyl aryl sulfonates (TFMS): An applicable trifluoromethoxylation reagent

Fluorine is probably another favorite hetero-atom for incorporation into small molecules after nitrogen. Among many fluorine-containing groups, trifluoromethyl aryl ethers (ArOCF3) have unique properties in drug design and are difficult to be synthesized, and many different methods were developed to prepare them. A novel one-pot synthesis of o-iodine-aryl trifluoromethyl ethers (ArOCF3I) was described by the reaction of trifluoromethoxylation and iodination with trifluoromethyl aryl sulfonates (TFMS) in this manuscript. The reaction conditions were optimized by screening different solvents, crown ethers, substrates and the ratios and the yields of products were in moderate to high yields (up to 86%).

Synthesis and reactivity studies of a new reagent, ethyltriphenylphosphonium tribromide

A new reagent, ethyltriphenyl phosphonium tribromide (ETPPTB), has been synthesized and studied. Results show that the reagent is quite efficient for various reactions such as organic bominations, acylations, and isothiocyanate preparation. Copyright

CANNABINOID RECEPTOR MODULATOR

A cannabinoid receptor modulator containing a compound represented by Formula (I0) wherein, X is an oxygen atom, etc., R° is an optionally substituted acylamino group, ring A0 is a benzene ring which may further have a substituent in addition to R°, and ring B is an optionally substituted 5-membered heterocycle, or a salt thereof or a prodrug thereof.