178055-99-7

Usage

Uses

Used in Organic Synthesis:
1-(2`,4`-Dimethoxy-biphenyl-4-yl)ethanone is utilized as a building block in organic synthesis, particularly for the creation of various pharmaceuticals and bioactive molecules. Its unique structure and functional groups make it a valuable component in the development of new compounds with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(2`,4`-Dimethoxy-biphenyl-4-yl)ethanone serves as a key intermediate for the synthesis of pharmaceuticals. Its presence in the molecular structure can influence the pharmacological properties of the final product, making it an essential component in drug design and development.
Used in Organic Chemistry Reactions:
Due to its versatile reactivity, 1-(2`,4`-Dimethoxy-biphenyl-4-yl)ethanone can also be employed as a reagent in various organic chemistry reactions. This allows for the modification and functionalization of other molecules, further expanding the compound's utility in chemical research and development.
Used in Materials Science:
1-(2`,4`-Dimethoxy-biphenyl-4-yl)ethanone has potential applications in materials science, where its unique properties can be harnessed to create novel materials with specific characteristics. These materials could have uses in various industries, such as electronics, aerospace, or automotive, depending on their properties.
Used as a Precursor for Specialty Chemicals:
Additionally, 1-(2`,4`-Dimethoxy-biphenyl-4-yl)ethanone can be used as a precursor for the production of specialty chemicals. These chemicals may have specific applications in various industries, such as fragrances, dyes, or coatings, where their unique properties can be leveraged for specific uses.

Upstream product

• 99-91-2 para-chloroacetophenone 
• 133730-34-4 2,4-dimethoxyphenylboronic acid 
• 64101-67-3 4-acetylphenyl p-toluenesulfonate 
• 99-93-4 4-Hydroxyacetophenone 
• 99-90-1 para-bromoacetophenone 

Relevant academic research and scientific papers

Suzuki-Miyaura coupling of aryl sulfonates with arylboronic acids using a morpholine-Pd(OAc)2 catalyst system

We report a new catalyst system, a morpholine-Pd(OAc)2 complex, for Suzuki-Miyaura coupling of aryl tosylates or mesylates with arylboronic acids to give biaryl compounds. The morpholine-Pd(OAc)2 catalyst system is proposed to be a precursor of the catalytically active species in the coupling reaction. Aryl chlorides and aryl triflates can also be used in this coupling reaction. Altogether, 22 biaryl compounds were obtained using this catalyst system. We report a new catalyst system, a morpholine-Pd(OAc) 2 complex, for Suzuki-Miyaura coupling of aryl tosylates or mesylates with arylboronic acids to give biaryl compounds. The morpholine-Pd(OAc) 2 catalyst system is proposed to be a precursor of the catalytically active species in the coupling reaction. Copyright

Palladium nanoparticles supported on polyaniline nanofibers as a semi-heterogeneous catalyst in water

(Chemical Equation Presented) A tandem catalyst for Suzuki coupling of activated or deactivated aryl chlorides and aryl boronic acids in water and for phenol synthesis from aryl chlorides in 1:1 water/dioxane was obtained by supporting palladium nanoparticles on polyaniline nanofibers (PANI; see TEM image). Thus, 2-phenylphenol was synthesized from 1,2-dichlorobenzene (see equation).

Structure-based design of (5-arylamino-2H-pyrazol-3-yl)-biphenyl-2′, 4′-diols as novel and potent human CHK1 inhibitors

The cocrystal structure of a library hit was used to design a novel series of CHK1 inhibitors. The new series retained the critical hydrogen-bonding groups of the resorcinol moiety for binding but lacked the phenolic anilide moiety. The newly designed com

AMINOPYRAZOLE COMPOUNDS AND USE AS CHK1 INHIBITORS

Described herein are aminopyrazole compounds of formula (I), wherein R1, R2, L and Ar are as defined in the specification. Such compounds are capable of modulating the activity of a checkpoint kinase and methods for utilizing such mo