68058-80-0

Usage

Uses

Used in Photodynamic Therapy:
(2,5-diphenyl-3H-pyrrol-3-ylidene)diazenium is used as a photosensitizer for its potential to activate drugs that target and kill cancer cells when exposed to light. Its unique structure and properties make it a promising candidate for the development of novel cancer treatment strategies.
Used in Nitric Oxide Release:
(2,5-diphenyl-3H-pyrrol-3-ylidene)diazenium is used as a nitric oxide-releasing agent due to its diazenium moiety, which has been studied for its ability to release nitric oxide. This signaling molecule has various physiological and therapeutic effects, making the compound an interesting target for further research in medicinal chemistry and drug development.

Upstream product

• 13219-95-9 3-amino-2,5-diphenylpyrrole 
• 75096-67-2 2,5-diphenyl-3-nitrosopyrrole 

Downstream Products

• 838-40-4 2,5-diphenyl-1H-pyrrole 
• 86864-11-1 3-methoxy-2,5-diphenyl-1H-pyrrole 
• 86864-00-8 2,5-diphenyl-3-(3-phenyl-2-propenyl)pyrrole 
• 86864-01-9 2,5-diphenyl-3-(1-phenyl-2-propenyl)pyrrole 
• 86864-03-1 2,5-diphenyl-3-(1-phenylpropyl)pyrrole 
• 86864-02-0 2,5-diphenyl-3-(3-phenylpropyl)pyrrole 
• 1889-67-4 dicumene 
• 86863-98-1 3-(1-methyl-1-phenylethyl)-2,5-diphenylpyrrole 
• 86864-04-2 3-(2,3-dimethyl-2-butenyl)-2,5-diphenylpyrrole 
• 86864-12-2 3-acetoxy-2,5-diphenylpyrrole 
• 70487-19-3 3-(4-methoxyphenyl)-2,5-diphenyl-1H-pyrrole 
• 86864-06-4 2,5-diphenyl-3-(2-methoxyphenyl)-1H-pyrrole 
• 70487-22-8 3-(o-cyanophenyl)-2,5-diphenylpyrrole 
• 70487-14-8 5-cyano-1,3-diphenyl-2H-cyclooctapyrrole 

Relevant academic research and scientific papers

3-Diazopyrroles. Part 5 (1). Antibacterial activity of 3-diazo-2-phenylpyrroles

3-Diazo-2-phenylpyrroles 3a-g showed antimicrobial activity against Gram-positive bacteria, whereas against Gram-negative strains the inhibitory activity is limited to derivatives 3a and 3c. The substituents at 4 and 5 positions strongly influence the inh

Studies in Organic Mass Spectrometry. VIII. The Elecron Impact Mass Spectra of 2,4-Substituted-3-diazo-5-phenylpyrroles

The electron impact mass spectra (75 eV) of the β-diazopyrroles always show the molecular ions and undergo as the main fragmentation process the elimination of nitrogen followed by ring opening reactions leading to benzonitrile either as neutral or charge

REACTIVITY OF 3-DIAZOPYRROLES. PART 2.

3-Diazopyrroles 8 were prepared as key compounds for an alternative route to synthetize 1H-pyrrolocinnoline. However under the acidic conditions, decomposition and intermolecular coupling reactions were only observed.