7196-81-8

Usage

Imidazole derivative

Five-membered ring with two nitrogen atoms 2,2,4,5-tetraphenyl-2H-imidazole is a derivative of imidazole, which is a five-membered ring structure containing two nitrogen atoms.

Tetraphenyl groups

Four phenyl groups attached to the imidazole ring The compound features four phenyl groups (a benzene ring with a hydrogen atom replaced by a side chain) attached to the imidazole ring, which contributes to its unique properties.

Potential applications

Organic synthesis and materials science Due to its unique structure and properties, 2,2,4,5-tetraphenyl-2H-imidazole has potential applications in the fields of organic synthesis and materials science.

Possible uses in pharmaceutical research

Therapeutic applications Although further studies are needed, 2,2,4,5-tetraphenyl-2H-imidazole may have potential uses in pharmaceutical research and development, exploring its possible therapeutic applications.

Significance in organic chemistry

Various applications in different industries As a notable compound in the realm of organic chemistry, 2,2,4,5-tetraphenyl-2H-imidazole has the potential for various applications across different industries.

Upstream product

• 108-86-1 bromobenzene 
• 588-59-0 stilbene 
• 57892-00-9 2,2,4,5-tetraphenyl-2H-imidazole 1-oxide 
• 143678-10-8 1,3-diaza-6-oxa-2,2,4,5-tetraphenylbicyclo<3.1.0>hex-3-ene 
• 73219-53-1 Benzhydryl-[2-[(E)-benzhydrylimino]-1,2-diphenyl-eth-(E)-ylidene]-amine 
• 111205-80-2 [2-[(E)-Benzhydrylimino]-1,2-diphenyl-eth-(E)-ylidene]-(1-phenyl-ethyl)-amine 

Downstream Products

• 13730-10-4 1,2,4,5-tetraphenyl-1H-imidazole 

Relevant academic research and scientific papers

Copper-catalyzed [2+3]-annulation of N-H imines with vinyl azides: Access to polyaryl 2: H -imidazoles

A practical method for the synthesis of 2H-imidazoles via a [2+3] annulation of N-H imines with vinyl azides using a copper catalyst is developed. In this conversion, environmentally friendly oxygen is used as the sole oxidant and N2 and H2O are the only by-products. The catalytic transformation, operating under mild conditions, is operationally simple and is considered as a readily available catalytic system having good substrate and functional compatibility with high atom-efficiency without the need for additional ligands or additives.

Photochemistry of Azole N-Oxides. Facile Photoisomerisation of 2H-Imidazole N-Oxides to 1,3-Diaza-6-oxabicyclohex-3-enes and Synthesis of a 1,3-Diaza-4,7-dioxatricyclo1,603,5>heptane

Ultraviolet irradiation of a series of 2H-imidazole N-oxides 2 has been shown to effect a clean isomerization to derivatives of the new ring system, 1,3-diaza-6-oxabicyclohex-3-ene, 7.Epoxidation of a representative 7 has given access to the hither

UNEXPECTED REACTIONS OF 1,4-DIAZA-1,3-DIENES UNDER ACYLATING CONDITIONS. A NEW CYCLIZATION TO NON-ACYLATED IMIDAZOLE DERIVATIVES

The reaction of anions from 1,2-bisimines with acid chlorides gives unacylated 2H-imidazoles.The unprecedented reactivity of these anions is interpreted by cyclization of the radical generated by electron transfer from the anion to the acid chloride.