28165-45-9

Usage

Uses

Used in Pharmaceutical Industry:
METHYL 3-BROMO-2-HYDROXYBENZOATE is used as an active ingredient for its potential therapeutic applications in the treatment of various diseases and conditions. Its antimicrobial properties contribute to its use in formulations that combat infections, while its antioxidant capabilities may support health and wellness applications.
Used in Cosmetic Industry:
In the cosmetic industry, METHYL 3-BROMO-2-HYDROXYBENZOATE is used as a key component in skin care products. It is valued for its ability to protect the skin from oxidative stress and microbial infections, thereby promoting healthier and more resilient skin.
Used in Topical Medications:
METHYL 3-BROMO-2-HYDROXYBENZOATE is utilized as an ingredient in topical medications due to its antimicrobial and antioxidant properties. It aids in the treatment of skin conditions by reducing inflammation and combating harmful microorganisms.
Used in Synthesis of Organic Compounds:
This chemical compound is also used in the synthesis of various organic compounds, serving as a building block for the creation of new molecules with potential applications in different fields.
It is crucial to handle METHYL 3-BROMO-2-HYDROXYBENZOATE with care due to its potential health risks if not properly managed, emphasizing the need for safety measures in its application and use.

Upstream product

• 67-56-1 methanol 
• 3883-95-2 3-bromosalicylic acid 
• 854914-90-2 3-bromo-2-hydroxy-thiobenzoic acid S-methyl ester 
• 95-56-7 2-hydroxybromobenzene 
• 119-36-8 methyl salicylate 
• 74-88-4 methyl iodide 

Downstream Products

• 28165-47-1 3-bromo-2-hydroxybenzamide 
• 942296-83-5 C₁₇H₁₄O₆Br₂ 
• 130883-74-8 3,3'-dibromo-5,5'-dicarboxy-4,4'-dihydroxydiphenylmethane 

Relevant academic research and scientific papers

ASK1 INHIBITING AGENTS

Provided are compounds of Formulas (I'), (I), (II') and (II), or pharmaceutically acceptable salts thereof, and methods for their use and production.

Facile p-toluenesulfonic acid-promoted para-selective monobromination and chlorination of phenol and analogues

para-Regioselective bromination of phenol and analogues, promoted by p-toluenesulfonic acid, is achieved in high to excellent yields at room temperature with N-bromosuccinimide. Chlorination with N-chlorosuccinimide and catalysed by p-toluenesulfonic acid also gives para-chlorinated phenol analogues in good yields at room temperature. para-Bromination of phenol, promoted by p-toluenesulfonic acid, is achieved in excellent yields at room temperature with N-bromosuccinimide. p-Toluenesulfonic acid is also effective as a promoter of para-chlorination with N-chlorosuccinimide.

A short and efficient preparation of methyl-[1,2,4]oxadiazolium derivatives with plant-inducing activity

A short and efficient preparation of methyl-[1,2,4]oxadiazolium derivatives with plant-inducing activity is discussed. A concise and efficient synthetic method leading to structurally diverse array of oxadiazolium derivatives, starting from halogenated phenols is also developed. The starting point of the synthesis is the Lewis acid mediated addition of isocyanates to phenols. The strategy also involves a new and rapid access to all meta-halogenated salicylic acids, compounds of high synthetic value.