145764-54-1

Basic information

• Product Name: 5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE
• Synonyms: 5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE;Tetrakisdihydroxyphenylporphine;5,10,15,20-tetrakis(3,5-dihydroxyphenyl)-21h,23h-porphine90+%;5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin
• CAS NO: 145764-54-1
• Molecular Formula: C44H30N4O8
• Molecular Weight: 742.73
• Product Categories: Biochemistry;Porphyrins
• Mol File: 145764-54-1.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• Density: 1.554g/cm³
• Refractive Index: 1.799
• CAS DataBase Reference: 5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE(145764-54-1)
• EPA Substance Registry System: 5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE(145764-54-1)

Safety Data

• Hazardous Substances Data: 145764-54-1(Hazardous Substances Data)

Usage

Description

5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE, also known as 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin, is a type of porphyrin compound characterized by its unique molecular structure. It possesses four 3,5-dihydroxyphenyl groups attached to the porphyrin core, which contributes to its distinct properties and potential applications in various fields.

Uses

Used in Biomedical Applications:
5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE is used as a key component in the development of porphyrin-based magnetic and fluorescent dual-modal nanoprobes for tumor imaging. These nanoprobes leverage the unique properties of the porphyrin compound to enhance the detection and monitoring of cancerous cells, providing valuable information for diagnosis and treatment planning.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of new drugs with potential applications in various therapeutic areas.
Used in Material Science:
5,10,15,20-TETRAKIS(3,5-DIHYDROXYPHENYL)-21H,23H-PORPHINE is also utilized in material science for the development of novel materials with specific optical, electronic, and magnetic properties. Its incorporation into these materials can lead to the creation of advanced materials with potential applications in various industries, such as electronics, energy, and sensing technologies.

InChI:InChI=1/C44H30N4O8/c49-25-9-21(10-26(50)17-25)41-33-1-2-34(45-33)42(22-11-27(51)18-28(52)12-22)36-5-6-38(47-36)44(24-15-31(55)20-32(56)16-24)40-8-7-39(48-40)43(37-4-3-35(41)46-37)23-13-29(53)19-30(54)14-23/h1-20,45,48-56H/b41-33-,41-35-,42-34-,42-36-,43-37-,43-39-,44-38-,44-40-

Upstream product

• 13682-61-6 potassium tetrachloroaurate(III) 
• 109-97-7 pyrrole 
• 26153-38-8 3,5-dihydroxybenzaldehyde 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 74684-34-7 5,10,15,20-tetrakis(3,5-dimethoxyphenyl)-21H,23H-porphine 

Relevant articles and documents

Ni(II) complex of octasubstituted tetraphenylporphine as a stationary phase for gas chromatography

The Ni(II) complex of 5,10,15,20-Tetrakis[3′,5′-di(2′′-methylbutyloxy)phenyl]porphine was synthesized and characterized by 1H NMR, UV-vis spectroscopy and MALDI-TOF mass-spectrometry. The stationary phase on the base of synthesized Ni(II) complex was used for chromatographic separation of isomeric methyl-And dimethylpyridines. The high structural selectivity of this sorbent was explained by giving the results of DFT calculation of pyridine derivatives axial complexes with porphyrin Ni(II) complexes.

Design of two-photon absorbing fluorophores for FRET antenna-core oxygen probes

Four two-photon absorbing fluorophores A1-A4 are reported and their spectroscopic properties are analyzed for use, in combination with palladium-porphyrinato complexes C1 and C2, as two-photon absorbing antennas and energy donors for FRET-based antenna-co

Fluorenyl dendrimer porphyrins: synthesis and photophysical properties

New symmetrical dendrimeric type super-porphyrin bearing sixteen fluorenyl donor groups sixteen fluorenylporphyrin SOFP (1) have been synthesized and characterized. Preliminary photophysical properties are reported; in comparison to the references first g

Functionally layered dendrimers: A new building block and its application to the synthesis of multichromophoric light-harvesting systems

(Chemical Equation Presented) A divergent synthesis of internally functionalized dendrimers based on a modular functional monomer has been developed. This strategy was applied to the construction of a light-harvesting dendrimer containing one set of napht

Preparation method of substituted aryl porphyrin

The invention provides a preparation method of substituted aryl porphyrin. The method comprises the following steps that a, aromatic aldehyde shown in the formula (1) is dissolved in a reaction solvent to obtain a dissolving solution; b, pyrrole is dropwi