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22112-77-2

  • Product Name:meso-Tetra (4-chlorophenyl) porphine
  • Molecular Formula:C44H26Cl4N4
  • Molecular Weight:752.529
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Product Details

pd_meltingpoint:>27 °C

Purity:99%

Chinese factory supply meso-Tetra (4-chlorophenyl) porphine 22112-77-2 in stock with high standard

  • Molecular Formula:C44H26Cl4N4
  • Molecular Weight:752.529
  • Melting Point:>27 °C 
  • PSA:56.30000 
  • Density:1.398g/cm3 
  • LogP:9.47980 

meso-Tetra (4-chlorophenyl) porphine(Cas 22112-77-2) Usage

General Description

Meso-tetra(4-chlorophenyl)porphine is a chemical compound that belongs to the group of porphyrins, which are heterocyclic macrocycles containing four pyrrole rings. meso-Tetra (4-chlorophenyl) porphine is a type of porphyrin that contains four 4-chlorophenyl groups attached to the pyrrole rings. It has been studied for its potential applications in photodynamic therapy, a treatment that uses light-sensitive compounds to selectively destroy cancer cells. Meso-tetra(4-chlorophenyl)porphine has also been investigated for its use in chemical sensors, catalysis, and as a model system for studying the properties of natural porphyrin compounds. Furthermore, it has been utilized in the synthesis of other porphyrin derivatives for various research and industrial purposes.

InChI:InChI=1/C44H26Cl4N4/c45-29-9-1-25(2-10-29)41-33-17-19-35(49-33)42(26-3-11-30(46)12-4-26)37-21-23-39(51-37)44(28-7-15-32(48)16-8-28)40-24-22-38(52-40)43(36-20-18-34(41)50-36)27-5-13-31(47)14-6-27/h1-24,49,52H/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-

22112-77-2 Relevant articles

Insights into the new cadmium(II) metalloporphyrin: Synthesis, X-ray crystal structure, Hirshfeld surface analysis, photophysical and cyclic voltammetry characterization of the (morpholine){(meso-tetra(para-chloro-phenyl)porphyrinato}cadmium(II)

Mchiri, Chadlia,Dhifaoui,Ezzayani, Khaireddine,Guergueb, Mouhieddinne,Roisnel, Thierry,Loiseau, Fredérique,Nasri

, p. 10 - 19 (2019)

In this work we report the synthesis of ...

UV–visible and fluorescence spectroscopic assessment of meso?tetrakis?(4?halophenyl) porphyrin; H2TXPP (X = F, Cl, Br, I) in THF and THF-water system: Effect of pH and aggregation behaviour

Dar, Umar Ali,Shah, Shakeel A.

, (2020)

The current study determines optical and...

A One-Step Route to CO2-Based Block Copolymers by Simultaneous ROCOP of CO2/Epoxides and RAFT Polymerization of Vinyl Monomers

Wang, Yong,Zhao, Yajun,Ye, Yunsheng,Peng, Haiyan,Zhou, Xingping,Xie, Xiaolin,Wang, Xianhong,Wang, Fosong

, p. 3593 - 3597 (2018)

The one-step synthesis of well-defined C...

Synthesis of novel single site tin porphyrin complexes and the catalytic activity of tin tetrakis(4-fluorophenyl)porphyrin over -caprolactone

Yaman, Hanifi,Kayan, Asgar

, p. 231 - 237 (2017)

Tin tetrakis(4-fluorophenyl)porphyrin, t...

Synthesis and single crystal structure of a new polymorph of 5, 10, 15, 20-tetrakis-(4-chlorophenyl) porphyrin, H2TTPCl4: Spectroscopic investigation of aggregation of H2TTPCl4

Dechan, Padma,Bajju, Gauri Devi,Sood, Puneet,Dar, Umar Ali

, p. 79 - 93 (2018)

5, 10, 15, 20-tetrakis-(4-chlorophenyl) ...

PH-switchable porphyrin receptor for binding halide ions

Ivanova, Yu. B.,Kulikova,Mamardashvili, N. Zh.

, p. 1231 - 1238 (2011)

Main properties of 5,10,15,20-tetra(4-ch...

Preparation of a porphyrin-polyoxometalate hybrid and its photocatalytic degradation performance for mustard gas simulant 2-chloroethyl ethyl sulfide

Tao, Fangsheng,Tian, Shubo,Wang, Yong'an,Yang, Ying,Zhang, Lijuan,Zhong, Yuxu,Zhou, Yunshan

supporting information, (2022/01/03)

By combining 5,10,15,20-tetra(4-chlorine...

Efficient oxidation of cycloalkanes with simultaneously increased conversion and selectivity using O2 catalyzed by metalloporphyrins and boosted by Zn(AcO)2: A practical strategy to inhibit the formation of aliphatic diacids

Shen, Hai-Min,Wang, Xiong,Ning, Lei,Guo, A-Bing,Deng, Jin-Hui,She, Yuan-Bin

, (2020/11/20)

The direct sources of aliphatic acids in...

Spectroscopic characterization, X-ray molecular structures and cyclic voltammetry study of two (piperazine) cobalt(II) meso-arylporphyin complexes. Application as a catalyst for the degradation of 4-nitrophenol

Al-Ghamdi, Youssef O.,Brahmi, Jihed,Guergueb, Mouhieddinne,Guerineau, Vincent,Loiseau, Frédérique,Molton, Florian,Nasri, Habib,Nasri, Soumaya,Roisnel, Thierry

, (2021/10/01)

Two new cobaltous-porphyrin complexes, n...

K2S2O8mediated synthesis of 5-Aryldipyrromethanes and meso-substituted A4-Tetraarylporphyrins

Laha, Joydev K.,Hunjan, Mandeep Kaur

, p. 664 - 673 (2021/06/03)

The synthesis of dipyrromethanes from py...

22112-77-2 Process route

pyrrole
109-97-7,30604-81-0

pyrrole

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

5,10,15,20-tetra-(4-chlorophenyl)porphyrin
22112-77-2

5,10,15,20-tetra-(4-chlorophenyl)porphyrin

Conditions
Conditions Yield
With vanadium(V) oxychloride; In dichloromethane; for 1h; Ambient temperature; other reagents: TiCl4, VO(OEt)Cl2, VO(OiPr)Cl2, Mn(OAc)3;
65%
With propionic acid; Reflux;
65%
pyrrole; 4-chlorobenzaldehyde; With boron trifluoride diethyl etherate; In chloroform; at 61 ℃; for 1h;
In chloroform; at 61 ℃; for 1h;
64%
With air; nitrobenzene; valeric acid; at 141 ℃; for 1h;
56%
With propionic acid; for 0.5h; Reflux;
56%
pyrrole; 4-chlorobenzaldehyde; In propionic acid; toluene; at 152.4 ℃; for 0.15h; under 2280.15 Torr; Large scale; Green chemistry;
With oxygen; In propionic acid; toluene; for 0.3h; under 1520.1 Torr; Large scale; Green chemistry;
52.2%
pyrrole; 4-chlorobenzaldehyde; With propionic acid; In toluene; at 152.4 ℃; for 0.15h; under 2280.15 Torr;
With oxygen; In toluene; for 0.3h; Reflux;
51.8%
With 1-methyl-3-nitrobenzene; propionic acid; valeric acid; for 2h; Reflux;
50.3%
With propionic acid; for 0.5h; Reflux;
41%
With hydrogenchloride; In N,N-dimethyl-formamide;
38%
With air; chloroacetic acid; In xylene; for 1.5h; Heating;
34.6%
pyrrole; 4-chlorobenzaldehyde; With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 0.5h;
With selenium(IV) oxide; In dichloromethane; at 20 ℃; for 1h;
34%
4-chlorobenzaldehyde; With benzoic acid; at 200 ℃; for 0.0833333h; under 2736.18 Torr;
pyrrole; at 200 ℃; for 0.333333h;
25%
pyrrole; 4-chlorobenzaldehyde; With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 0.5h;
With selenium(IV) oxide; In dichloromethane; for 1h;
24%
pyrrole; 4-chlorobenzaldehyde; With Tulsion-63 resin; Triethyl orthoacetate; In dichloromethane; at 20 ℃; for 17h;
With chloranil; In dichloromethane; for 2h; Heating;
23%
With propionic acid; at 165 ℃; for 1h; Inert atmosphere; Schlenk technique; Reflux;
23.1%
With acetic acid; Reflux;
21%
With propionic acid; for 2h; Reflux;
20%
pyrrole; 4-chlorobenzaldehyde; With trifluoroacetic acid; In dichloromethane; at 25 ℃; for 1h; Inert atmosphere;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; for 1h;
20.8%
With propionic acid; for 0.5h; Reflux;
20%
at 200 ℃; for 0.25h;
10%
With air; propionic acid; for 0.0666667h; microwave irradiation;
7%
With propionic acid; In nitrobenzene; at 120 ℃; for 1h;
In propionic acid; nitrobenzene; at 120 ℃; for 1h;
With propionic acid; for 30h; Heating;
With chloranil; trifluoroacetic acid; Yield given. Multistep reaction; 1) CH2Cl2, 2 h, r.t., 2) 1 h, reflux;
With chloranil; aluminum oxide; FSM-16(2.8 nm); Yield given. Multistep reaction; 1) CH2Cl2, r.t., 1 h, 2) CH2Cl2, 45 deg C, 1 h;
In propionic acid; Heating;
With trifluoroacetic acid; In dichloromethane; water; for 2h;
With propionic acid; for 2h; Reflux;
pyrrole; 4-chlorobenzaldehyde; With boron trifluoride diethyl etherate; In chloroform; at 20 ℃; for 1h; Inert atmosphere;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone;
pyrrole; 4-chlorobenzaldehyde; With trifluoroacetic acid; In dichloromethane; for 1h; Darkness; Inert atmosphere;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; for 1h; Inert atmosphere;
In propionic acid; for 0.666667h; Reflux;
With propionic acid; for 0.5h; Reflux;
With propionic acid; for 0.5h; Reflux;
With propionic acid; for 1h; Reflux;
pyrrole; 4-chlorobenzaldehyde; With trifluoroacetic acid; In dichloromethane; for 1h; Inert atmosphere; Schlenk technique; Darkness;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; for 1h; Inert atmosphere; Schlenk technique; Darkness;
With propionic acid; Reflux;
In propionic acid; at 145 ℃; for 2h; Inert atmosphere; Darkness;
With propionic acid; at 145 ℃; for 2h; Inert atmosphere; Darkness;
With propionic acid; for 0.75h; Reflux;
5,10,15,20-tetrakis(4-chlorophenyl)porphyrinogen
248606-50-0

5,10,15,20-tetrakis(4-chlorophenyl)porphyrinogen

5,10,15,20-tetra-(4-chlorophenyl)porphyrin
22112-77-2

5,10,15,20-tetra-(4-chlorophenyl)porphyrin

Conditions
Conditions Yield
With air; In dichloromethane; at 39 ℃; for 4h;
With air; In dichloromethane; at 39 ℃;
With air; In dichloromethane; at 39 ℃; for 3h;
for 2h; UV-irradiation;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; for 2h; Inert atmosphere; Darkness;
117 mg
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In dichloromethane; at 39 ℃;
With ammonium cerium (IV) nitrate; In dichloromethane; at 20 ℃; for 0.333333h; Green chemistry;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; for 0.0833333h; Inert atmosphere;

22112-77-2 Upstream products

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    109-97-7

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  • 104-88-1
    104-88-1

    4-chlorobenzaldehyde

  • 22112-84-1
    22112-84-1

    tetrakis(4-aminophenyl)porphyrin

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