26733-16-4

Usage

Uses

Used in Organic Synthesis:
(3,5-dibromo-4-hydroxyphenyl)(phenyl)methanone is used as a key intermediate in organic synthesis for the production of various chemical compounds and pharmaceuticals. Its unique structure allows for versatile reactions and modifications, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
(3,5-dibromo-4-hydroxyphenyl)(phenyl)methanone is used as a starting material in pharmaceutical research for the development of new drugs. Its potential biological activities, such as antioxidant and antibacterial properties, make it a promising candidate for the treatment of various diseases and conditions.
Used in Antioxidant Applications:
(3,5-dibromo-4-hydroxyphenyl)(phenyl)methanone is used as an antioxidant in various industries, including food, cosmetics, and pharmaceuticals. Its ability to scavenge free radicals and protect against oxidative damage makes it a valuable additive in these applications.
Used in Antibacterial Applications:
(3,5-dibromo-4-hydroxyphenyl)(phenyl)methanone is used as an antibacterial agent in various settings, such as in the development of new antibiotics or as a preservative in consumer products. Its ability to inhibit bacterial growth makes it a useful tool in combating bacterial infections.
Used in Photoinitiator Applications:
(3,5-dibromo-4-hydroxyphenyl)(phenyl)methanone is used as a photoinitiator in polymerization reactions, particularly in the production of polymers and coatings. Its ability to absorb light and initiate chemical reactions makes it a valuable component in the synthesis of various polymeric materials.
Used in Medicinal Chemistry:
(3,5-dibromo-4-hydroxyphenyl)(phenyl)methanone is used in medicinal chemistry for the development of new therapeutic agents. Its potential role in the treatment of certain diseases and conditions, as well as its unique chemical properties, make it an interesting subject of study for researchers in this field.

Upstream product

• 1137-42-4 4-Hydroxybenzophenone 
• 615-58-7 2,4-dibromophenol 
• 98-07-7 Benzotrichlorid 
• 118-79-6 2,4,6-tribromophenol 
• 52751-69-6 4-benzyl-2,6-dibromo-phenol 
• 107-21-1 ethylene glycol 
• 26733-18-6 4-amino-3,5-dibromo-benzophenone 
• 611-94-9 4-Methoxybenzophenone 
• 98-88-4 benzoyl chloride 
• 108-95-2 phenol 
• 1137-41-3 (4-aminophenyl)(phenyl)methanone 
• 871893-39-9 4-ethoxy-3,5-dibromo-benzophenone 

Relevant academic research and scientific papers

An eco-friendly Co(OAc)2-catalyzed aerobic oxidation of 4-benzylphenols into 4-hydroxybenzophenones

An undecorated Co(OAc)2-catalyzed aerobic oxidation system has been reported that enables direct transformation of 4-benzylphenols into the corresponding 4-hydroxybenzophenones. The procedure is especially suitable for electron-withdrawing group-containing substrates, which are commonly inefficient to conduct this category of oxidation. Based on well-defined p-benzoquinone methides and the confirmed ethereal intermediate, a plausible mechanism was depicted.

Synthesis, biochemical evaluation and rationalisation of a series of 3,5- dibromo derivatives of 4-hydroxyphenyl ketone-based compounds as probes of the active site of type 3 of 17β-hydroxysteroid dehydrogenase (17β-hsd3) and the role of hydrogen bonding interaction in the inhibition of 17β-HSD3

We report the synthesis, evaluation and rationalisation of the inhibitory activity of a series of 3,5-dibromo derivatives of 4-hydroxyphenyl ketone as probes of the active site of the type 3 of 17β-hydroxysteroid dehydrogenase (17β-HSD3). The results support the important role of hydrogen bonding interaction in the inhibition of 17β-HSD3.

Regioselective and high-yielding bromination of aromatic compounds using hexamethylenetetramine-bromine

A regioselective and highly efficient method for bromination of aromatic compounds in the presence of a stoichiometric amount of hexamethylenetetramine- bromine (HMTAB) as an efficient reagent in dichloromethane is reported. The selectivity depends on the temperature and nature of the substituent on the substrate. The reactivity of this reagent was increased by supporting it to silica gel for bromination of less activated compounds.

Alkaline Condensation of Benzotrichloride with Bromophenols

The reaction of benzotrichloride with 4-alkylphenols is of potential industrial importance to sythesize 2-hydroxy-5-alkylbenzophenones which are industrial oxime extractants used for extraction of copper and other metals.The attempts to obtain 2-hydroxychlorobenzophenone derivatives from 4-chlorophenol and 2,4-dichlorophenol, respectively and benzotrichloride yields besides 2-hydroxychlorobenzophenone, hydroxyketones having fewer atoms of chlorine in the aromatic ring as well as hydroxychlorobenzophenones resulting from the migration of chlorine from the para to the ortho position.In the present paper the reaction between benzotrichloride and bromophenols is studied.