1147092-75-8

Upstream product

• 116412-87-4 (3,4-dimethoxyl phenyl)(4-methylphenyl)methanone 
• 104-87-0 4-methyl-benzaldehyde 
• 122775-35-3 3,4-Dimethoxyphenylboronic acid 
• 91-16-7 1,2-dimethoxybenzene 
• 874-60-2 4-methyl-benzoyl chloride 

Downstream Products

• 1147092-59-8 (3,4-dimethoxyphenyl)-(4-morpholin-4-ylmethylphenyl)methanone 
• 1147092-62-3 (3,4-dimethoxyphenyl)-{4-[(methylprop-2-ynylamino)methyl]phenyl}methanone 
• 1147092-63-4 [4-(3,4-dihydro-1H-isoquinolin-2-ylmethyl)phenyl]-(3,4-dimethoxyphenyl)methanone 
• 1147092-78-1 4-(3,4-dimethoxybenzoyl)benzaldehyde 
• 1147092-69-0 (4-{[benzyl-(2-dimethylaminoethyl)amino]methyl}phenyl)-(3,4-dimethoxyphenyl)methanone 
• 1147092-65-6 (3,4-dimethoxyphenyl)-(4-{[(2-methoxybenzyl)methylamino]methyl}phenyl)methanone 
• 1147092-64-5 (3,4-dimethoxyphenyl)-(4-{[methyl-(3-nitrobenzyl)amino]methyl}phenyl)methanone 
• 1147092-66-7 (3,4-dimethoxyphenyl)-(4-{[methyl-(3-methylbenzyl)amino]methyl}phenyl)methanone 
• 1147092-67-8 {4-[(benzylethylamino)methyl]phenyl}-(3,4-dimethoxyphenyl)methanone 
• 1147092-61-2 (3,4-dimethoxyphenyl)-(4-{[(2-dimethylaminoethyl)methylamino]methyl}phenyl)methanone 
• 1147092-60-1 C₂₀H₂₅NO₃ 
• 1147092-68-9 (4-{[benzyl-(2-hydroxyethyl)amino]methyl}phenyl)-(3,4-dimethoxyphenyl)methanone 

Relevant academic research and scientific papers

Visible light-driven direct synthesis of ketones from aldehydes via C[sbnd]H bond activation using NiCu nanoparticles adorned on carbon nano onions

An efficient, straightforward and high yield synthetic approach is described for the direct synthesis of diaryl ketones via the C[sbnd]H bond activation of aldehydes using NiCu nanoparticles adorned on carbon nano onions as an efficient heterogeneous catalyst under the irradiation of a mercury-vapor lamp (400 w) via simple workup. This C[sbnd]H bond activation reaction appears simple and convenient with a wide substrate scope in view of its excellent synthesis prowess as illustrated in the preparation of new-approved anti-Alzheimer and anti-HIV medicinal compounds under greener and mild reaction conditions; catalyst could be recycled and reused five times without any loss of catalytic activity.

Benzophenones as xanthone-open model CYP11B1 inhibitors potentially useful for promoting wound healing

The inhibition of steroidogenic cytochrome P450 enzymes has been shown to play a central role in the management of life-threatening diseases such as cancer, and indeed potent inhibitors of CYP19 (aromatase) and CYP17 (17α hydroxylase/17,20 lyase) are curr

Design, synthesis, and evaluation of benzophenone derivatives as novel acetylcholinesterase inhibitors

Starting from a structure-based drug design, new acetylcholinesterase inhibitors were designed and synthesized as analogues of donepezil. The compounds were composed by an aromatic function and a tertiary amino moiety connected by a suitable spacer. In pa