93325-15-6

Basic information

• Product Name: 2,5-diphenyl-1H-pyrrole-3-carboxylic acid
• CAS NO: 93325-15-6
• Molecular Formula: C₁₇H₁₃NO₂
• Molecular Weight: 263.2906
• Mol File: 93325-15-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 491°C at 760 mmHg
• Flash Point: 250.7°C
• Density: 1.248g/cm³
• Vapor Pressure: 1.86E-10mmHg at 25°C
• Refractive Index: 1.648
• CAS DataBase Reference: 2,5-diphenyl-1H-pyrrole-3-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-diphenyl-1H-pyrrole-3-carboxylic acid(93325-15-6)
• EPA Substance Registry System: 2,5-diphenyl-1H-pyrrole-3-carboxylic acid(93325-15-6)

Safety Data

• Hazardous Substances Data: 93325-15-6(Hazardous Substances Data)

Usage

Synonym

Diphenylpyrrolecarboxylic acid
Another name for the same compound, highlighting its structure.

Derivative of pyrrole

A compound that is structurally related to pyrrole, a five-membered aromatic ring with one nitrogen atom.

Contains two phenyl groups

Two phenyl groups (a ring of six carbon atoms with delocalized electrons) are attached to the pyrrole ring, influencing the compound's properties.

Potential use in various fields

The compound has been studied for its possible applications in different areas, such as medicine and materials science.

Unique structure and properties

The combination of the pyrrole ring and the two phenyl groups gives the compound distinct characteristics that make it interesting for research and development.

Promising candidate for applications

Due to its structure and properties, the compound is considered a potential candidate for use in drug development, organic semiconductors, and advanced materials.

Ongoing research

Further studies are being conducted to explore the compound's potential uses and properties, indicating that its full potential is not yet fully understood or utilized.

Upstream product

• 61795-22-0 (1-azidoethene-1,2-diyl)dibenzene 
• 952-06-7 deoxybenzoin oxime 
• 451-40-1 phenyl benzyl ketone 
• 16483-98-0 2,3-diphenyl-2H-azirine 
• 13901-70-7 dimethyl 2,5-diphenyl-1H-pyrrole-3,4-dicarboxylate 
• 70-11-1 α-bromoacetophenone 
• 65474-26-2 ethyl 2,5-diphenyl-1H-pyrrole-3-carboxylate 
• 29113-48-2 ethyl 2-benzoyl-4-oxo-4-phenylbutanoate 

Downstream Products

• 130850-67-8 3,4-Dibromo-2,5-diphenyl-1H-pyrrole 
• 130850-62-3 4-Bromo-2,5-diphenyl-1H-pyrrole-3-carboxylic acid 

Relevant articles and documents

Visible-light-induced formal [3+2] cycloaddition for pyrrole synthesis under metal-free conditions

A photocatalytic formal [3+2] cycloaddition of 2H-azirines with alkynes has been achieved under irradiation by visible light in the presence of organic dye photocatalysts. This transformation provides efficient access to highly functionalized pyrroles in good yields and has been applied to the synthesis of drug analogues. A primary trial of photocascade catalysis merging energy transfer and redox neutral reactions was shown to be successful. Photo(chemistry) op: A photocatalytic formal [3+2] cycloaddition of 2H-azirines with alkynes has been established under the irradiation of visible light in the presence of an organic dye. This transformation provides efficient access to highly functionalized pyrroles in good yields and has been applied to the formal synthesis of an inhibitor for HMG-CoA reductase.