13901-75-2

Basic information

• Product Name: 1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone
• CAS NO: 13901-75-2
• Molecular Formula: C₂₄H₁₉NO
• Molecular Weight: 337.4138
• Mol File: 13901-75-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 534.5°C at 760 mmHg
• Flash Point: 275.7°C
• Density: 1.143g/cm³
• Vapor Pressure: 1.68E-11mmHg at 25°C
• Refractive Index: 1.626
• CAS DataBase Reference: 1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone(13901-75-2)
• EPA Substance Registry System: 1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone(13901-75-2)

Safety Data

• Hazardous Substances Data: 13901-75-2(Hazardous Substances Data)

Usage

General Description

1-(2,4,5-triphenyl-1H-pyrrol-3-yl)ethanone, also known as triphenylpyrrole, is a chemical compound with a distinct and complex structure. It is classified as an aryl ketone and belongs to the pyrrole group of chemicals. Triphenylpyrrole is commonly used as a building block in organic synthesis and as a precursor for various pharmaceuticals and agrochemicals. It possesses interesting properties such as fluorescence and biological activity, making it an important molecule in chemical research and industry. Additionally, triphenylpyrrole has potential applications in materials science, particularly in the development of functional materials and dyes. Overall, this chemical compound is of significant interest in various fields due to its unique structure and versatile properties.

Upstream product

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

Downstream Products

• 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 
• 102754-20-1 1-(2,4,5-triphenyl-pyrrol-3-yl)-ethanone oxime 
• 102543-54-4 (2,4,5-triphenyl-pyrrol-3-yl)-glyoxal 

Relevant articles and documents

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.

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