190198-12-0

Usage

Uses

Used in Pharmaceutical Industry:
1-(2,4-DIMETHOXY-PHENYL)-1H-IMIDAZOLE is used as a building block for the synthesis of complex compounds due to its unique structure and properties. Its potential applications in this industry include the development of new drugs and pharmaceuticals, leveraging its imidazole derivative nature and the presence of methoxy groups on the phenyl ring.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(2,4-DIMETHOXY-PHENYL)-1H-IMIDAZOLE is used as a chemical intermediate for the development of various agrochemical products. Its structure and properties make it a valuable component in the synthesis of compounds with potential applications in agriculture, such as pesticides, herbicides, and other related products.
Used in Materials Science:
1-(2,4-DIMETHOXY-PHENYL)-1H-IMIDAZOLE is utilized as a versatile building block in materials science for the synthesis of advanced materials with specific properties. Its unique structure and the presence of methoxy groups on the phenyl ring make it a promising candidate for the development of materials with tailored characteristics for various applications, such as electronics, coatings, and adhesives.
Used as a Drug Lead:
Due to its potential biological activity, 1-(2,4-DIMETHOXY-PHENYL)-1H-IMIDAZOLE may be used as a drug lead in the pharmaceutical industry. Its structure and properties could be further explored and modified to develop new drugs with specific therapeutic effects, targeting various medical conditions and diseases.
Used as a Precursor in Pharmaceutical Production:
1-(2,4-DIMETHOXY-PHENYL)-1H-IMIDAZOLE can also serve as a precursor in the production of pharmaceuticals. Its unique structure and properties make it a valuable starting point for the synthesis of more complex and biologically active compounds, which can be further developed into effective drugs for various therapeutic applications.

Upstream product

• 288-32-4 1H-imidazole 
• 17715-69-4 1-Bromo-2,4-dimethoxybenzene 
• 530-62-1 1,1'-carbonyldiimidazole 
• 50-00-0 formaldehyd 
• 131543-46-9 Glyoxal 
• 2735-04-8 2,4-Dimethoxyaniline 
• 20469-63-0 1-iodo-2,4-dimethoxybenzene 

Relevant academic research and scientific papers

Molecular Engineering of Iridium Blue Emitters Using Aryl N-Heterocyclic Carbene Ligands

The synthesis of a new series of neutral bis[2-(2′,4′-difluorophen-2′-yl)pyridine][1-(2′-aryl)-3-methylimidazol-2-ylidene]iridium(III) complexes is reported. Each complex has been characterized by NMR spectroscopy, UV/Vis spectrophotometry, and cyclic vol

Iridium complexes of N-heterocyclic carbene ligands: Investigation into the energetic requirements for efficient electrogenerated chemiluminescence

A series of five heteroleptic Ir(III) complexes of the general form Ir(ppy)2(C∧C:) have been prepared (C∧C represents a bidentate cyclometalated phenyl-substituted imidazolylidene ligand). The five complexes arise from the

A new, efficient and recyclable lanthanum(III) oxide-catalyzed C-N cross-coupling

A new and efficient protocol for the C-N cross-coupling of aryl halides with heteroaromatic amines in the presence of lanthanum(III) oxide (10 mol%) as a recyclable catalyst, N,N′-dimethylethylenediamine (DMEDA) (20 mol%) and potassium hydroxide (KOH) as a base in dimethyl sulfoxide (DMSO) at 110 °C has been developed. This inexpensive catalytic system is highly effective towards the amination of aryl halides with various nitrogen nucleophiles and is significantly tolerant towards other functional groups in the substrates. Copyright

Ligand-free copper-catalyzed arylation of imidazole and N,N′-carbonyldiimidazole, and microwave-assisted synthesis of N-Aryl-1H-imidazoles

Microwave-assisted arylation of 1H-imidazoles and N,N′- carbonyldiimidazole under ligand-free copper-mediated conditions in tetraethyl orthosilicate is reported. Valuable evidence for understanding of the Cu-catalyzed mechanism of the Ullmann reaction is

Amino acid promoted CuI-catalyzed C-N bond formation between aryl halides and amines or N-containing heterocycles

CuI-catalyzed coupling reaction of electron-deficient aryl iodides with aliphatic primary amines occurs at 40 °C under the promotion of N-methylglycine. Using L-proline as the promoter, coupling reaction of aryl iodides or aryl bromides with aliphatic primary amines, aliphatic cyclic secondary amines, or electron-rich primary arylamines proceeds at 60-90 °C; an intramolecular coupling reaction between aryl chloride and primary amine moieties gives indoline at 70 °C; coupling reaction of aryl iodides with indole, pyrrole, carbazole, imidazole, or pyrazole can be carried out at 75-90 °C; and coupling reaction of electron-deficient aryl bromides with imidazole or pyrazole occurs at 60-90 °C to provide the corresponding N-aryl products in good to excellent yields. In addition, N,N-dimethylglycine promotes the coupling reaction of electron-rich aryl bromides with imidazole or pyrazole to afford the corresponding N-aryl imidazoles or pyrazoles at 110 °C. The possible action of amino acids in these coupling reactions is discussed.