13901-75-2

Usage

Uses

Used in Organic Synthesis:
1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone is used as a building block in organic synthesis for its ability to form a variety of complex molecules and contribute to the development of new chemical entities.
Used in Pharmaceutical Industry:
1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone is used as a precursor for various pharmaceuticals due to its unique structure and properties, which can be utilized in the creation of novel drugs with potential therapeutic applications.
Used in Agrochemicals:
1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone is used as a precursor in the development of agrochemicals, where its properties can be harnessed to create new compounds with applications in agriculture, such as pesticides or fertilizers.
Used in Materials Science:
Triphenylpyrrole is used in materials science for the development of functional materials and dyes, leveraging its fluorescence and other properties to create materials with specific characteristics for various applications.

Upstream product

• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 123-54-6 acetylacetone 
• 93-91-4 1-phenylbutan-1,3-dione 
• 100-52-7 benzaldehyde 
• 16483-98-0 2,3-diphenyl-2H-azirine 

Downstream Products

• 102543-54-4 (2,4,5-triphenyl-pyrrol-3-yl)-glyoxal 
• 102754-20-1 1-(2,4,5-triphenyl-pyrrol-3-yl)-ethanone oxime 
• 3274-61-1 2,4,5-triphenylpyrrole 
• 98304-68-8 2,4,5-triphenyl-pyrrole-3-carboxylic acid 
• 103404-19-9 2-(2,4,5-triphenyl-pyrrol-3-yl)-quinoxaline 

Relevant academic research and scientific papers

Nickel-catalyzed formal [3 + 2]-cycloaddition of 2H-azirines with 1,3-dicarbonyl compounds for the synthesis of pyrroles

An efficient nickel-catalyzed formal [3 + 2]-cycloaddition of 2H-azirines with 1,3-dicarbonyl compounds for the synthesis of tetrasubstituted pyrroles has been developed. This transformation involves cleavage of the C[dbnd]N double bond and the construction of new C[sbnd]C and C[sbnd]N bonds. The reaction employs readily available starting materials, tolerates a wide range of functional groups, and affords tetrasubstituted pyrroles in good to high yields under mild reaction conditions. A gram-scale reaction was performed to demonstrate the scale-up applicability of this synthetic method.

Cocamidopropyl betaine catalyzed benzoin condensation and pseudo-four-component reaction of the in situ formed benzoin in water

An improved synthesis of benzoins, as key synthetic building blocks, and substituted pyrroles in micelle medium using a very small amount of cocamidopropyl betaine in water is described. In this one-pot strategy, benzoin condensation of aldehydes and further pseudo-four-component reaction of the in situ formed benzoin with 1,3-dicarbonyls, and ammonium acetate gave excellent yields of the desired pyrrole products.

Molybdate sulfuric acid as a reusable solid catalyst in the synthesis of 2,3,4,5-tetrasubstituted pyrroles via a new one-pot [2+2+1] strategy

Molybdate sulfuric acid (MSA) has been found as an efficient and reusable solid acid catalyst for the synthesis of new 2,3,4,5-tetrasubstituted pyrroles via a novel [2+2+1] strategy. Thus, one-pot three-component reaction of benzoin derivatives, 1,3-dicar