125237-08-3

Usage

Uses

Used in Disinfectant and Antiseptic Applications:
2-Bromo-3,5-dimethylphenol is used as a disinfectant and antiseptic due to its potent antimicrobial properties, which are effective against a wide range of microorganisms. It plays a crucial role in maintaining hygiene and preventing the spread of infections in various settings.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-Bromo-3,5-dimethylphenol serves as an important intermediate in the synthesis of various drugs. Its unique chemical structure allows for the development of new therapeutic agents with potential applications in treating different medical conditions.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 2-Bromo-3,5-dimethylphenol is utilized in the production of a variety of chemical compounds. Its versatility in chemical reactions makes it a valuable building block for creating new molecules with diverse applications.
Used in Medical Applications:
2-Bromo-3,5-dimethylphenol has been studied for its potential use in the treatment of bacterial infections. Its antimicrobial activity makes it a promising candidate for developing new antibiotics or other treatments to combat resistant bacterial strains.
Used in Personal Care Products:
In the personal care industry, 2-Bromo-3,5-dimethylphenol is used as a preservative in various products. Its ability to inhibit the growth of microorganisms helps maintain the stability and safety of these products, ensuring their longevity and preventing contamination.
It is important to handle 2-Bromo-3,5-dimethylphenol with care, as it is considered hazardous if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken during its production, use, and disposal to minimize potential risks.

Upstream product

• 108-68-9 3,5-Dimethylphenol 

Relevant academic research and scientific papers

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%).

Selectivity enhancement of aromatic halogenation reactions at the micellar interface: Effect of highly ionic media

Halogenation (iodination and bromination) of various aromatic compounds has been studied in micellar media in order to observe the effect on regioselectivity and conversion of the reaction. The addition of surfactant causes a change in the chemical shifts of the aromatic proton resonance of phenol which proves the orientation of the aromatic compound on the micellar surface. However, increase in ionic strength of the reaction media affects the selectivity of reaction by disturbing this spatial orientation of the aromatic compound in the micelle. Selectivity towards particular isomers is dependent on the concentration of the surfactant. In bromination of chlorobenzene (deactivated aromatic compound) enhancement in selectivity and conversion towards the para isomer has been observed.

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

Benzofuran derivatives

The present invention provides a compound represented by the following formula (I): wherein: Ring A represents an optionally substituted piperazine ring, an optionally substituted morpholine ring, or an optionally substituted homopiperazine ring;R1 and R2 are the same or different from each other, and represent a hydrogen atom or optionally substituted lower alkyl;R3 and R4 are the same or different from each other, and represent a hydrogen atom or halogenated or non-halogenated lower alkyl;R5 to R7 are the same or different from each other, and represent a hydrogen atom, hydroxy, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkoxy, optionally substituted cycloalkyl, optionally substituted aryl, an optionally substituted aromatic heterocyclic ring, optionally substituted amino, or acyl; and represents a single bond or double bond, or a salt thereof.

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.

Hindered organoboron groups in organic chemistry. 27. Preparations and some properties of alkylbis(2,6-dimethyl-4-methoxyphenyl)boranes ((DMP)2BR)

Akylbis(2,6-dimethyl-4-methoxyphenyl)boranes ((DMP)2BR) have been synthesized in an attempt to overcome the limitations of the steric hindrance approach to the production of boron stabilised carbanions. Anion production from (DMP)2BR, followed by alkylations and condensations with aldehydes are reported. Reduction of (DMP)2F with potassium hydride yields the corresponding hydroborate. Attempts to isolate (DMP)2BH were unsuccessful but the borane was readily trapped with alkynes, yielding alkenylboranes. The allyl derivative, (DMP)2BAllyl, was made and some of its reactions were investigated.