33757-34-5

Usage

Uses

Used in Organic Synthesis:
(3-BromoPhenyl)(4-Methylphenyl)Methanol is used as a building block in organic synthesis for creating more complex molecules. Its unique structure allows for various chemical reactions to produce a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-BromoPhenyl)(4-Methylphenyl)Methanol is used as a reagent in chemical reactions, contributing to the development of new drugs and therapeutic agents.
Used as a Precursor in Drug Production:
(3-BromoPhenyl)(4-Methylphenyl)Methanol serves as a precursor in the production of various pharmaceutical drugs, playing a crucial role in the synthesis of active pharmaceutical ingredients.
Used in Biological Activity Studies:
(3-BroMophenyl)(4-Methylphenyl)Methanol has been studied for its potential biological activities, which may lead to the discovery of new therapeutic agents and treatments for various diseases and conditions.

Upstream product

• 102092-51-3 3-bromo-4′-methylbenzophenone 
• 3132-99-8 m-bromobenzoic aldehyde 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 108-36-1 1,3-dibromobenzene 
• 104-87-0 4-methyl-benzaldehyde 
• 13028-93-8 4-CH₃-C₆H₄Na 
• 106-43-4 para-chlorotoluene 
• 5720-05-8 4-methylphenylboronic acid 

Downstream Products

• 32038-94-1 {2-[(3-Bromo-phenyl)-p-tolyl-methoxy]-ethyl}-dimethyl-amine 
• 917077-70-4 1-[3-[hydroxy(4-methylphenyl)methyl]phenyl]ethanone 
• 917077-73-7 1-[3-[4-(azidomethyl)benzoyl]phenyl]ethanone 
• 917077-72-6 1-[3-[4-(bromomethyl)benzoyl]phenyl]ethanone 
• 917077-71-5 1-[3-(4-methylbenzoyl)phenyl]ethanone 

Relevant academic research and scientific papers

Orthoplatinated triarylphosphite as a highly efficient catalyst for addition reactions of arylboronic acids with aldehydes: Low catalyst loading catalysis and a new tandem reaction sequence

(Chemical Equation Presented) Readily available, air/moisture-stable orthoplatinated triarylphosphite catalyzes the addition reactions of arylboronic acids with aldehydes with the catalyst loading as low as 0.01%. It also cataylzes a new tandem reaction of arylboronic acids with α,β- unsaturated aldehydes to form 1,3-diaryl-1-propanols. Our study provides a new paradigm for the application of orthoplatinated triarylphosphites, and may pave the road to develop other Pt(II) catalysts for such addition reactions and other tandem reactions with such addition reactions as part of the reaction sequence.

Biotinylated biphenyl ketone-containing 2,4-dioxobutanoic acids designed as HIV-1 integrase photoaffinity ligands

The diketo acid (DKA) class of HIV-1 integrase inhibitors are thought to function by chelating divalent metal ions within the enzyme catalytic center. However, differences in mutations conferring resistance among sub-families of DKA inhibitors suggest tha

Process for producing benzhydrols

There is disclosed a process for producing benzhydrls by reacting an arylmetal compound with an aromatic aldehyde. According to this process, benzhydrols useful as raw materials for medicines and photopolymerization initiators can be produced in a high yield and industrially advantageously.