32431-36-0

Usage

Uses

Used in Research and Pharmaceutical Industry:
2,3-dimethyl-2,3-dihydroisoquinoline is utilized as a compound with potential biological activities, such as antiviral and antitumor properties. It is being studied for its possible applications in the development of treatments for various diseases.
Used in Neurodegenerative Disease Treatment:
2,3-dimethyl-2,3-dihydroisoquinoline is being investigated for its potential role in the treatment of neurodegenerative diseases, such as Parkinson's and Alzheimer's, due to its possible biological activities that could be beneficial in managing these conditions.
Used in Organic Synthesis:
2,3-dimethyl-2,3-dihydroisoquinoline serves as a building block in the synthesis of various organic compounds, making it a valuable component in the creation of new chemical entities.
Used in Chemical Production:
2,3-dimethyl-2,3-dihydroisoquinoline can be produced through chemical reactions, such as Friedel-Crafts alkylation, which allows for its synthesis and incorporation into a wide range of applications across different industries.

Upstream product

• 1125-80-0 3-methylisoquinoline 
• 74-88-4 methyl iodide 

Downstream Products

• 34140-16-4 2-methyl-3-(3-nitro-trans-styryl)-isoquinolinium; iodide 
• 54365-72-9 2,3-Dimethyl-1,2,3,4-tetrahydroisoquinoline 
• 109726-75-2 2-methyl-3-trans-styryl-isoquinolinium; iodide 
• 7114-78-5 2,3-Dimethyl-1-oxo-1,2-dihydroisoquinoline 
• 1125-80-0 3-methylisoquinoline 
• 2216-67-3 2-N-methylaminonaphthalene 
• 2437-03-8 2-ethylaminonaphthalene 
• 135-19-3 β-naphthol 
• 51650-27-2 1-benzyl-3-methylisoquinoline 
• 113164-18-4 3-(4-dimethylamino-trans-styryl)-2-methyl-isoquinolinium; iodide 

Relevant academic research and scientific papers

Electrochemical regioselective selenylation/oxidation of: N-alkylisoquinolinium salts via double C(sp2)-H bond functionalization

An efficient, novel, and environmentally friendly electrochemical regioselective selenylation/oxidation of N-alkylisoquinolinium salts via double C(sp2)-H bond functionalization under undivided electrolytic conditions has been developed. A series of selenide isoquinolones were easily accessed through this sustainable and clean electrochemical system. The present protocol was further extended to afford selenide quinolones and 1,3-dimethyl-1H-benzo[d]imidazol-2(3H)-ones. Furthermore, antiviral bioassays demonstrated that compound 3j exhibited excellent antiviral activity against tobacco mosaic virus (TMV), and its inhibition rate was up to 90%. This journal is

Syntheses of quaternary carbon-containing oxazatricycle and spiropyran libraries via multicomponent reactions and their molecular switching properties

A practical protocol for the preparation of parallel solution-phase libraries of the quaternary carbon-containing oxazatricycles and spiropyrans is reported. Target compounds were obtained in moderate to excellent yields by an Et3N-mediated mul

Transfer hydrogenation of isoquinolinium salts catalyzed by a rhodium complex

Regio- and chemoselective transfer hydrogenation of isoquinolinium salts catalyzed by [Cp*RhCl2]2 using HCOOH-Et3N (5:2) as a hydrogen source was realized. A variety of N-methyl- and N-benzyl-1,2,3,4-tetrahydroisoquinoline

Dyeing method using a specific cationic derivative and a compound selected among a specific aldehyde, a specific ketone, a quinone and a di-imino-isoindoline or 3-amino-isoindolone derivative

Compositions, methods, and kits for dyeing at least one keratin fiber, comprising at least one specific cationic compound and at least one compound chosen from specific aldehydes, specific ketones, quinones, diiminoisoindoline derivatives, and 3-aminoisoindolone derivatives, with the proviso that the inventive compositions do not comprise an oxidizing agent.

Indium metal as a reducing agent in organic synthesis

The low first ionisation potential (5.8 eV) of indium coupled with its stability towards air and water, suggest that this metallic element should be a useful reducing agent for organic substrates. The use of indium metal for the reduction of C=N bonds in imines, the heterocyclic ring in benzo-fused nitrogen heterocycles, of oximes, nitro compounds and conjugated alkenes and the removal of 4-nitrobenzyl protecting groups is described. Thus the heterocyclic ring in quinolines, isoquinolines and quinoxalines is selectively reduced using indium metal in aqueous ethanolic ammonium chloride. Treatment of a range of aromatic nitro compounds under similar conditions results in selective reduction of the nitro groups; ester, nitrile, amide and halide substituents are unaffected. Likewise indium in aqueous ethanolic ammonium chloride is an effective method for the deprotection of 4-nitrobenzyl ethers and esters. Indium is also an effective reducing agent under non-aqueous conditions and α-oximino carbonyl compounds can be selectively reduced to the corresponding N-protected amine with indium powder, acetic acid in THF in the presence of acetic anhydride or di-tert-butyl dicarbonate. Conjugated alkenes are also reduced by indium in THF-acetic acid.