1056451-68-3

Usage

Chemical class

Isoquinoline derivative

Substitution

Substituted phenyl group at the 1-position

Structure

Symmetrical with two benzene rings fused to an isoquinoline ring

Physical state

Pale yellow solid

Melting point

86-89°C

Potential applications

Pharmaceutical research

Possible studies

Biological activities and pharmacological properties

Upstream product

• 19493-44-8 1-chloroisoquinoline 
• 172975-69-8 3,5-dimethylphenyl boronic acid 
• 657408-07-6 dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane 
• 84110-40-7 Dihydroxy-isobutyl-boran 
• 1443013-16-8 4,6-dichloro-1-(3,5-dimethylphenyl)isoquinoline 
• 119-65-3 isoquinoline 
• 34696-73-6 3,5-dimethyphenylmagnesium bromide 
• 1532-72-5 isoquinoline N-oxide 
• 556-96-7 5-bromo-1,3-xylene 

Relevant academic research and scientific papers

Red phosphorescent compound, and organic electroluminescent device using same

The invention discloses a red phosphorescent compound, and an organic electroluminescence device using the same. The organic electroluminescent device comprises an anode, a hole injection layer, a hole transporting layer, a luminescent layer, an electron

Red light metal complex, preparation method and application thereof

The invention belongs to the field of organic electroluminescence materials, and discloses a red light metal complex formed by using an alkyl-substituted phenylisoquinoline derivative as a main ligand, a preparation method and an application thereof. Different alkyl substituents are introduced on the main ligand, purification and sublimation yields of a material are remarkably improved, so using cost of the material is effectively reduced, and it is extremely beneficial to industrial production. In addition, because of the steric-hindrance effect of an increased alkyl chain, steric hindrance of molecules is enhanced, so a luminescence quenching situation is relieved, and luminous efficiency is improved.

Novel Organic Light Emitting Materials

Novel phosphorescent metal complexes containing 2-phenylisoquinoline ligands with at least two substituents on the isoquinoline ring are provided. The disclosed compounds have low sublimation temperatures that allow for ease of purification and fabrication into a variety of OLED devices.

TMEDA-assisted effective direct ortho arylation of electron-deficient N -heteroarenes with aromatic grignard reagents

In the addition of TMEDA in toluene, aryl Grignards could effectively and site-specifically ortho-arylate electron-deficient heteroarenes under mild conditions. This endeavor successfully changed the old low-yielding reaction, aryl Grignard addition to N-heteroarenes, into an efficient procedure for heterobiaryls. The combination of the inexpensive aryl Grignards, TMEDA, the cost-free air, no use of any transition-metal catalyst, the mild reaction conditions, and the high-yielding gram-scale results enables this new procedure to be cost-effective and potentially utilizable in industry.