5068-23-5

Usage

Uses

Used in Pharmaceutical Industry:
6,7-diethoxy-1-[4-methoxy-3-(1-methylethyl)phenyl]-1,2,3,4-tetrahydroisoquinoline is used as a potential drug lead for the development of new medications due to its possible biological activity.
Used in Chemical Research:
6,7-diethoxy-1-[4-methoxy-3-(1-methylethyl)phenyl]-1,2,3,4-tetrahydroisoquinoline is utilized in chemical research as a building block for the synthesis of complex organic molecules, given its unique structure and potential reactivity.
Used in Organic Synthesis:
6,7-diethoxy-1-[4-methoxy-3-(1-methylethyl)phenyl]-1,2,3,4-tetrahydroisoquinoline is used as a key intermediate in the synthesis of various organic compounds, contributing to the advancement of organic chemistry.

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 4559-70-0 Diphenylphosphine oxide 
• 87199-17-5 4-formylphenylboronic acid, 
• 102185-58-0 4-(triphenylphosphonio)phenolate 

Downstream Products

• 63403-56-5 1-(4-dimethylaminophenyl)-2-(4-diphenylphosphinoylphenyl)ethene 
• 5068-18-8 4-(diphenylphosphino)benzaldehyde 

Relevant academic research and scientific papers

Palladium anchored on a covalent organic framework as a heterogeneous catalyst for phosphorylation of aryl bromides

A simple azine-linked covalent organic framework (COF) with high thermal and chemical stabilities has been prepared by using deep eutectic solvent (DES) as green media. The as-synthesized COF was employed as heterogeneous ligand for immobilization of PdII. The obtained Pd-supported COF nanoparticles catalyst (defined as Pd/TFPT-Azine-COF) was found to be an efficient heterogeneous catalyst for the Hirao reaction of aryl halides and dialkyl phosphites or diphenylphosphine oxide with excellent recyclability, reusability, and retention of crystallinity.

Palladium-catalyzed air-based oxidative coupling of arylboronic acids with H-phosphine oxides leading to aryl phosphine oxides

We present a novel and highly efficient methodology that allows for the construction of C-P bonds via the palladium-catalyzed air-based oxidative coupling of various commercially available arylboronic acids with easily oxidized H-phosphine oxides leading to valuable aryl phosphine oxides, particularly triarylphosphine oxides, with the use of air as the green oxidant, broad substrate applicability and good to excellent yields. The described catalytic system should be an efficient complement to the Chan-Lam type reaction and be useful in synthetic programs. This journal is the Partner Organisations 2014.