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

Uses

5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin (cas# 145764-54-1) is a porphyrin which has been used in the preparation of porphyrin-based magnetic and fluorescent dual-modal nanoprobes for tumor imaging.

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

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

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