Cas no 87345-22-0 (4-(10,15,20-Triphenyl-5-porphyrinyl)phenol)

4-(10,15,20-Triphenyl-5-porphyrinyl)phenol is a porphyrin derivative featuring a phenolic substituent, enhancing its solubility and reactivity for applications in catalysis, photodynamic therapy, and materials science. Its extended π-conjugation and functional group versatility make it valuable for designing advanced molecular systems, sensors, and light-harvesting materials. The compound exhibits strong absorption in the visible spectrum.
4-(10,15,20-Triphenyl-5-porphyrinyl)phenol structure
87345-22-0 structure
Product Name:4-(10,15,20-Triphenyl-5-porphyrinyl)phenol
CAS No:87345-22-0
MF:C44H30N4O
MW:630.735209941864
CID:1878404
Update Time:2025-06-17

4-(10,15,20-Triphenyl-5-porphyrinyl)phenol Chemical and Physical Properties

Names and Identifiers

    • 4-(10,15,20-Triphenylporphyrin-5-yl)phenol
    • 5,10,15-triphenyl-20-(4-hydroxyphenyl)porphyrin
    • phenol, 4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)-
    • LogP</sup>
    • 5,10,15-triphenyl-20-(4-hydroxyphenyl)-21H,23H-porphyrin
    • 4-(10,15,20-Triphenyl-21H,23H-porphyrin-5-yl)phenol
    • 4-(10,15,20-Triphenyl-5-porphyrinyl)phenol
    • 4-(10,15,20-Triphenyl-21H,23H-porphin-5-yl)phenol (ACI)
    • 5-(4-Hydroxylphenyl)-10,15,20-triphenylporphyrin
    • 5-(4-Hydroxyphenyl)-10,15,20-triphenylporphine
    • 5-(4-Hydroxyphenyl)-10,15,20-triphenylporphyrin
    • 5-(4-Hydroxyphenyl)-10,15,25-triphenylporphyrin
    • 5-(p-Hydroxyphenyl)-10,15,20-triphenyl-21H,23H-porphyrin
    • 5-(p-Hydroxyphenyl)-10,15,20-triphenylporphyrin
    • meso-5-(4′-Hydroxyphenyl)-10,15,20-triphenylporphyrin
    • Phenol, 4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)- 4-(10,15,20-triphenylporphyrin-5-yl)phenol
    • 5-(4-hydroxyphenyl)-10,15,20-triphenyl porphine
    • 5-(4-hydroxyphenyl)-10,15,20-(triphenyl)porphyrin
    • DK7583
    • Inchi： 1S/C44H30N4O/c49-32-18-16-31(17-19-32)44-39-26-24-37(47-39)42(29-12-6-2-7-13-29)35-22-20-33(45-35)41(28-10-4-1-5-11-28)34-21-23-36(46-34)43(30-14-8-3-9-15-30)38-25-27-40(44)48-38/h1-27,45,48-49H/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-
    • InChI Key： QMONKZRPMBDZDY-LWQDQPMZSA-N
    • SMILES： C1(O)=CC=C(C2=C3N=C(C(C4=CC=CC=C4)=C4NC(=C(C5=CC=CC=C5)C5=NC(=C(C6=CC=CC=C6)C6NC2=CC=6)C=C5)C=C4)C=C3)C=C1 |c:16,t:5,19,30|

Computed Properties

  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 49
  • Rotatable Bond Count: 4
  • Complexity: 1040
  • Topological Polar Surface Area: 77.6

Experimental Properties

  • Density: 1.290±0.06 g/cm3(Predicted)
  • Melting Point: >300 °C(Solv: chloroform (67-66-3); ligroine (8032-32-4))

4-(10,15,20-Triphenyl-5-porphyrinyl)phenol Pricemore >>

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4-(10,15,20-Triphenyl-5-porphyrinyl)phenol Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Potassium carbonate ,  Potassium iodide Solvents: Dimethylformamide ;  3 d, 80 °C; 80 °C → rt
Reference
Chemoselective epoxidation of dienes using polymer-supported manganese porphyrin catalysts
Brule, Emile; et al, Tetrahedron, 2004, 60(28), 5913-5918

Production Method 2

Reaction Conditions
1.1 Reagents: Praseodymium (hydroxyphenyl-triphenylporphyrin complex) ;  30 min, rt
1.2 Solvents: Acetone ;  20 min, rt
Reference
Synthesis and characterization of praseodymium-porphyrin by solid state reaction
Ma, Mingyou; et al, Jishou Daxue Xuebao, 2009, 30(3), 83-85

Production Method 3

Reaction Conditions
1.1 Solvents: Propionic acid
Reference
Rotaxane Type Complexation Behavior of Cyclodextrins with Zinc(II) Tetraphenylporphyrin-Viologen Linked Compounds
Ujiie, Tomomi; et al, Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2002, 42(3-4), 301-311

Production Method 4

Reaction Conditions
1.1 Reagents: Potassium hydroxide Solvents: Methanol ,  Water ;  5 h, reflux; reflux → rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  pH 4, rt
Reference
A facile synthesis and cytotoxicity of a novel porphyrin-cryptolepine conjugate
Kumar, Dalip; et al, Chemistry & Biology Interface, 2012, 2(2), 114-121

Production Method 5

Reaction Conditions
1.1 Reagents: Sodium methoxide Solvents: Methanol ,  Tetrahydrofuran ;  6 h, reflux
Reference
Kinetics and mechanisms of hydrolysis of tetraphenylporphyrins tethered to silicate glass via a primary or tertiary alcohol linker
Furuta, Nao; et al, Tetrahedron, 2014, 70(29), 4336-4342

Production Method 6

Reaction Conditions
1.1 Reagents: Hydrochloric acid ;  4 h, 60 °C
1.2 Reagents: Sodium carbonate Solvents: Water ;  neutralized
Reference
Synthesis of porphyrin glycoconjugates bearing thiourea, thiocarbamate and carbamate connecting groups: Influence of the linker on chemical and photophysical properties
Dallagnol, Juliana C. C.; et al, Dyes and Pigments, 2014, 107, 69-80

Production Method 7

Reaction Conditions
1.1 Solvents: Dichloromethane ;  15 min, 0 °C
1.2 Reagents: Boron tribromide Solvents: Dichloromethane ;  1 h, 0 °C; 18 h, rt
1.3 Reagents: Sodium carbonate Solvents: Dichloromethane ,  Water ;  neutralized, rt
Reference
Comparison between 5,10,15,20-Tetraaryl- and 5,15-Diarylporphyrins as Photosensitizers: Synthesis, Photodynamic Activity, and Quantitative Structure-Activity Relationship Modeling
Banfi, Stefano; et al, Journal of Medicinal Chemistry, 2006, 49(11), 3293-3304

Production Method 8

Reaction Conditions
1.1 Reagents: Boron tribromide Solvents: Dichloromethane
1.2 Reagents: Methanol
1.3 Reagents: Sodium carbonate Solvents: Water
1.4 Solvents: Chloroform
Reference
Synthesis and complexation properties of an oligooxaethylene-spacered porphyrin dimer. Toward the construction of a new switchable porphyrin array
Monti, Donato; et al, European Journal of Organic Chemistry, 1999, (8), 1901-1906

Production Method 9

Reaction Conditions
1.1 Solvents: Propionic acid ;  rt → 140 °C; 1 h, 140 °C
Reference
The syntheses of phthalocyanine hybrid derivatives and their properties
Kim, Seong Jin; et al, Kongop Hwahak, 2013, 24(3), 266-273

Production Method 10

Reaction Conditions
1.1 Reagents: Propionic acid ;  45 min, reflux
Reference
An NIR-triggered drug release and highly efficient photodynamic therapy from PCL/PNIPAm/porphyrin modified graphene oxide nanoparticles with the Janus morphology
Khoee, Sepideh; et al, RSC Advances, 2019, 9(68), 39780-39792

Production Method 11

Reaction Conditions
1.1 Reagents: Sulfuric acid Solvents: Water ;  0 °C
1.2 Reagents: Sodium nitrite Solvents: Water ;  10 min, 0 - 5 °C; 0 °C → rt; 20 min, rt
1.3 Reagents: Sulfuric acid Solvents: Water ;  10 min, 100 °C; 100 °C → rt
Reference
Regiospecific aryl nitration of meso-tetraarylporphyrins: The directive effect of para-substituent
Zhang, Hong-Liang; et al, Heterocycles, 2005, 65(12), 3001-3006

Production Method 12

Reaction Conditions
1.1 Catalysts: Palladium diacetate ,  Bis(1,1-dimethylethyl)[2′,4′,6′-tris(1-methylethyl)[1,1′-biphenyl]-2-yl]phosphin… Solvents: Tetrahydrofuran ;  25 °C; 12 h, 25 °C
1.2 Reagents: Hydrochloric acid Solvents: Methanol ,  Water ;  5 min, 25 °C
Reference
Palladium-catalyzed cross-coupling reactions of brominated porphyrins with functionalized organomagnesium reagents: Direct preparation of functional-group-bearing free base porphyrins
Sugita, Noriaki; et al, Heterocycles, 2016, 93(2), 483-511

4-(10,15,20-Triphenyl-5-porphyrinyl)phenol Raw materials

4-(10,15,20-Triphenyl-5-porphyrinyl)phenol Preparation Products

4-(10,15,20-Triphenyl-5-porphyrinyl)phenol Related Literature

87345-22-0 (4-(10,15,20-Triphenyl-5-porphyrinyl)phenol) Related Products

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