151256-86-9

Basic information

• Product Name: 5,15-dibromo-10,20-diphenylporphine
• Synonyms: 5,15-dibromo-10,20-diphenylporphine
• CAS NO: 151256-86-9
• Molecular Formula: C32H20Br2N4
• Molecular Weight: 620.336
• Product Categories: Porphyrins
• Mol File: 151256-86-9.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 932.0±65.0 °C(Predicted)
• Appearance: /
• Density: 1.581±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 5,15-dibromo-10,20-diphenylporphine(CAS DataBase Reference)
• NIST Chemistry Reference: 5,15-dibromo-10,20-diphenylporphine(151256-86-9)
• EPA Substance Registry System: 5,15-dibromo-10,20-diphenylporphine(151256-86-9)

Safety Data

• Hazardous Substances Data: 151256-86-9(Hazardous Substances Data)

Usage

General Description

5,15-dibromo-10,20-diphenylporphine is a chemical compound that belongs to the class of porphyrins, which are heterocyclic macrocycles composed of four pyrrole rings. This particular porphyrin contains two bromine atoms at positions 5 and 15, as well as two phenyl groups at positions 10 and 20. Porphyrins are known for their intense absorption of light, making them useful in various applications such as photodynamic therapy and as photosensitizers in solar cells. The presence of bromine atoms in this compound may impart specific chemical reactivity and properties, making it potentially useful in organic synthesis or other chemical processes. Overall, 5,15-dibromo-10,20-diphenylporphine is a significant compound with potential applications in various fields of science and technology.

Upstream product

• 22112-89-6 5,15-diphenylporphyrin 
• 100-52-7 benzaldehyde 
• 128-08-5 N-Bromosuccinimide 
• 75-09-2 dichloromethane 
• 21211-65-4 di(pyrrol-2-yl)methane 
• 118762-53-1 (Z)-2-(phenyl(2H-pyrrol-2-ylidene)methyl)-1H-pyrrole 

Downstream Products

• 156821-65-7 [5,15-bis(ethynyl)-10,20-diphenylporphinato]zinc(II) 
• 156821-56-6 5,15-bis(trimethylsilylethynyl)-10,20-diphenylporphyrin zinc(II) 
• 193265-36-0 (5,15-dibromo-10,20-diphenylporphyrinato)nickel(II) 
• 193265-38-2 5-bromo-15-nitro-10,20-diphenylporphyrinatonickel(II) 
• 193265-33-7 5,15-nitro-10,20-diphenylporphyrinatonickel(II) 
• 1315250-66-8 5,15-dibromo-10,20-diphenylporphyrin iron(III) chloride 

Relevant articles and documents

Metal-catalyzed direct heteroarylation of C-H (: Meso) bonds in porphyrins: Facile synthesis and photophysical properties of novel meso -heteroaromatic appended porphyrins

A simple and rapid microwave-assisted synthesis of heteroaromatic appended porphyrins using the Pd/Cu-catalyzed C-C coupling of meso-bromoporphyrins with various five- and six-membered heteroaromatic azoles has been successfully developed. The prepared he

General and Scalable Approach to A2B- and A2BC-Type Porphyrin Phosphonate Diesters

A two-step reaction sequence for accessing meso-(dialkoxyphosphoryl)porphyrins from readily available trans-A2-type porphyrins was developed. This approach involves bromination and subsequent palladium-catalyzed phosphonylation. Optimal conditi

Solvent-dependent moulding of porphyrin-based nanostructures: solid state, solution and on surface self-assembly

A novel porphyrin derivative 1?Zn was synthesised in order to mimic the self-assembly properties of natural light-harvesting antennas and its self-assembly behaviour in solution and in solid state were studied by NMR and X-Ray spectroscopies. The self-assembly of this molecule was triggered in apolar solvents and studied in solution by UV-Vis spectroscopy, suggesting it is able to form slipped face-to-face aggregates, or J-aggregates. The nanoscopic and microscopic morphology of the aggregates was elucidated by atomic force microscopy, revealing the formation of extended two-dimensional structures.