5-(4-hydroxyphenyl)-10,15,20-triphenyl porphine

Product Number: M40874; CAS Number: 87345-22-0

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5-(4-hydroxyphenyl)-10,15,20-triphenyl porphine CAS: 87345-22-0 MDL: MFCD09038998

Molecular weight: 630.735 g/mol

Molecular Formula: C44H30N4O

CAS Number: 87345-22-0

Storage: Store at room temperature, protect from light.

Synonyms: 4-(10,15,20-Triphényl-5-porphyrineyl)phénol,  4-(10,15,20-Triphenyl-5-porphyrinyl)phenol, 4-(10,15,20-Triphenyl-5-porphyrinyl)phenol, 4-(10,15,20-Triphenylporphyrin-5-yl)phenol, 4-[(1Z,7Z,12Z,16Z)-7,12,17-Triphenyl-21,22,23,24-tetraazapentacyclo[16.2.1.13,6.18,11.113,16]tetracosa-1,3,5,7,9,11(23),12,14,16,18(21),19-undecaen-2-yl]phenol, 5,10,15-triphenyl-20-(4-hydroxyphenyl)porphyrin, Phenol, 4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)-, 4-(10,15,20-Triphenyl-21H,23H-porphin-5-yl)phenol, 5-(4-hydroxylphenyl)-10,15,20-triphenylporphyrin, 5-(4-HYDROXYPHENYL)-10,15,20-TRIPHENYL PORPHINE, 5-(4-Hydroxyphenyl)-10,15,20-triphenyl-21H,23H-porphine, 5-(4-hydroxyphenyl)-10,15,20-triphenylporphyrin, 5-(羟苯基)- 10,15,20-苯基卟啉, 5,10,15-triphenyl-20-(4-hydroxyphenyl)-21H,23H-porphyrin, 87345-22-0, H2TPP(OH), MFCD09038998

Fields of Interest: Synthetic Porphyrins, Mono Functionalized Porphyrins

Background: 5-(4-hydroxyphenyl)-10,15,20-triphenyl porphine is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals.

References:

1.) Cheng, et al. Red Light-Triggered Intracellular Carbon Monoxide Release Enables Selective Eradication of MRSA Infection. Angew. Chem. Int. Ed.Volume 60, Issue 24. June 7, 2021, Pages 13513-13520.https://doi.org/10.1002/anie.202104024

2.) Ruan, et al. The synthesis of star-shaped poly(N-isopropylacrylamide) with two zinc porphyrins as the core and end groups via ATRP and “CLICK” chemistry and a photocatalytic performance study. New J. Chem., 2020, 44, 2781-2787. https://doi.org/10.1039/C9NJ05802H

3.) Rojas-Montoya, et al. Synthesis and photophysical properties of novel pyrene–metalloporphyrin dendritic systems. Dalton Trans., 2019,48, 10435-10447. https://doi.org/10.1039/C9DT00855A

4.) D’Souza, et al. Energy Transfer Followed by Electron Transfer in a Supramolecular Triad Composed of Boron Dipyrrin, Zinc Porphyrin, and Fullerene:  A Model for the Photosynthetic Antenna-Reaction Center ComplexJ. Am. Chem. Soc. 2004, 126, 25, 7898–7907. https://doi.org/10.1021/ja030647u

5.) Ngen, et al. Evaluation of delocalized lipophilic cationic dyes as delivery vehicles for photosensitizers to mitochondria. Bioorganic & Medicinal Chemistry. Volume 17, Issue 18, 15 September 2009, Pages 6631-6640. https://doi.org/10.1016/j.bmc.2009.07.074

6.) Wang, et al. Novel phosphoramidates with porphine and nitrogenous drug: One-pot synthesis and orientation to cancer cells. European Journal of Medicinal Chemistry. Volume 45, Issue 3, March 2010, Pages 890-895.

 

Categories

Porphyrins

Porphyrin Substitution

Hydroxy-Phenyl Substituted Porphyrins, Meso-Substituted Porphyrins, Phenyl Substituted Porphyrins

Porphyrin Family

A3B Porphyrins, Free Base Porphyrins, Hydroxy Porphyrins, Hydroxy-Phenyl Porphyrins, Tetra-Phenyl Porphine Derivatives

Functional Groups

Hydroxy, Hydroxyl

Purity %

>95%

Molecular Formula

C44H30N4O

Molecular Weight

630.735

CAS #

87345-22-0

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