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14527-51-6

  • Product Name:5,10,15,20-TETRA-P-TOLYL-21H,23H-PORPHINE
  • Molecular Formula:C48H38N4
  • Molecular Weight:670.857
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Product Details

pd_meltingpoint:>300℃

Purity:99%

Chinese Manufacturer supply 5,10,15,20-TETRA-P-TOLYL-21H,23H-PORPHINE 14527-51-6 in stock with high standard

  • Molecular Formula:C48H38N4
  • Molecular Weight:670.857
  • Melting Point:>300℃ 
  • Refractive Index:1.673 
  • PSA:56.30000 
  • Density:1.207 g/cm3 
  • LogP:8.09980 

5,10,15,20-TETRA-P-TOLYL-21H,23H-PORPHINE(Cas 14527-51-6) Usage

InChI:InChI=1/C48H38N4/c1-29-5-13-33(14-6-29)45-37-21-23-39(49-37)46(34-15-7-30(2)8-16-34)41-25-27-43(51-41)48(36-19-11-32(4)12-20-36)44-28-26-42(52-44)47(40-24-22-38(45)50-40)35-17-9-31(3)10-18-35/h5-28,49-50H,1-4H3/b45-37-,45-38-,46-39-,46-41-,47-40-,47-42-,48-43-,48-44-

14527-51-6 Relevant articles

Design and synthesis of porphyrins bearing catechols

Drexler, Cathy,Hosseini, Mir Wais,De Cian, Andre,Fischer, Jean

, p. 2993 - 2996 (1997)

The synthesis of meso-tetraarylporphyrin...

Cyclotriphosphazene ring as a platform for multiporphyrin assemblies

Rao, M. Rajeswara,Gayatri,Kumar, Amit,Sastry, G. Narahari,Ravikanth

, p. 3488 - 3496 (2009)

A simple method has been employed to syn...

Unexpected one-pot synthesis of A3-type unsymmetrical porphyrin

Mahmood, Mian Hr,Liu, Hai-Yang,Wang, Hua-Hua,Jiang, Yi-Yu,Chang

, p. 5853 - 5856 (2013)

The first direct synthesis of A3-type un...

Solution Characterization of Copper(II) and Silver(II) Porphyrins and the One-Electron Oxidation Products by Nuclear Magnetic Resonance Spectroscopy

Godziela, Gregory M.,Goff, Harold M.

, p. 2237 - 2243 (1986)

The Cu(II) and Ag(II) complexes of tetra...

Tetraphenylporphyrin derivatives possessing piperidine group as potential agents for photodynamic therapy

Liao, Ping-Yong,Gao, Ying-Hua,Wang, Xin-Rong,Bao, Lei-Lei,Bian, Jun,Hu, Tai-Shan,Zheng, Mei-Zhen,Yan, Yi-Jia,Chen, Zhi-Long

, p. 213 - 219 (2016)

Photodynamic therapy (PDT) is a noninvas...

Thiaporphyrins with one, two and four unsubstituted meso-carbons: Synthesis and functionalization

Agarwal, Neeraj,Hung,Ravikanth

, p. 3730 - 3734 (2003)

Thiaporphyrins with one, two and four un...

Novel fullerene receptors based on calixarene-porphyrin conjugates

Ká?, Martin,Lang, Kamil,Stibor, Ivan,Lhoták, Pavel

, p. 477 - 481 (2007)

Several different synthetic approaches e...

Cobalt Porphyrin-Polypyridyl Surface Coatings for Photoelectrosynthetic Hydrogen Production

Beiler,Khusnutdinova,Wadsworth,Moore

, p. 12178 - 12185 (2017)

Hybrid materials that link light capture...

FSM-16: Recyclable Mesoporous Acid Promoter for meso-Tetraarylporphyrin Synthesis

Shinoda, Tomotaka,Izumi, Yusuke,Onaka, Makoto

, p. 1801 - 1802 (1995)

A new porous silicate, FSM-16 with a por...

Structurally controlled porphyrin-aggregation process in phospholipid membranes

Borovkov, Victor V.,Anikin, Michael,Wasa, Kiyotaka,Sakata, Yoshiteru

, p. 477 - 482 (1996)

Structurally controlled aggregation cour...

Synthesis of meso-furyl porphyrins with N4, N3S, N2S2 and N3O porphyrin cores

Gupta, Iti,Ravikanth, Mangalampalli

, p. 6131 - 6139 (2003)

A series of meso-furyl porphyrins with f...

Synthesis and characterization of new molecular complexation between free base meso-tetraarylporphyrins and nitrosonium ion as π-acceptor

Molaei, Halimeh,Dehghani, Hossein

, p. 133 - 136 (2012)

NOBF4 reacts with para-substituted meso-...

Synthesis and characterization of tetraarylporphyrins in the presence of nano-TiCl4·SiO2

Zamani, Leila,Mirjalili, Bi Bi Fatemeh

, p. 578 - 581 (2015)

[MediaObject not available: see fulltext...

Preparation of pure meso-tetraphenylporphine and two derivatives.

Bhatti,Bhatti,Imbler,Lee,Lorenzen

, p. 307 - 309 (1972)

-

Beneficial effects of salts on an acid-catalyzed condensation leading to porphyrin formation

Li, Feirong,Yang, Kexin,Tyhonas, John S.,MacCrum, Kristy A.,Lindsey, Jonathan S.

, p. 12339 - 12360 (1997)

Addition of one of a variety of salts to...

Clay-Mediated meso-Tetraarylporphyrin Synthesis

Onaka, Makoto,Shinoda, Tomotaka,Izumi, Yusuke,Nolen, Ernest

, p. 2625 - 2628 (1993)

meso-Tetraphenylporphyrin syntheses from...

Phenomenological statistical physics modeling of metalloporphyrins adsorption at the molecular level

Aouaini, Fatma,Ben Yahia, Mohamed,M. Alanazi, Meznah

, (2021)

This paper is aimed to investigate the c...

Diboryl and diboranyl porphyrin complexes: Synthesis, structural motifs, and redox chemistry: Diborenyl porphyrin or diboranyl isophlorin?

Weiss, Andre,Hodgson, Michael C.,Boyd, Peter D. W.,Siebert, Walter,Brothers, Penelope J.

, p. 5982 - 5993 (2007)

The syntheses of diboryl porphyrin compl...

Structural elucidation and study of intermolecular interactions in meso-tetratolylporphyrins

Soman, Rahul,Sujatha, Subramaniam,Arunkumar, Chellaiah

, p. 833 - 842 (2016)

Synthesis and crystal structure analysis...

Ionic liquids for tetraarylporphyrin preparation

Kitaoka, Satoshi,Nobuoka, Kaoru,Ishikawa, Yuichi

, p. 7678 - 7685 (2005)

In place of widely used dichloromethane,...

SYNTHESIS AND CHARACTERIZATION OF A DIRECTLY LINKED PORPHYRIN-ANTHRAQUINONE MOLECULE

Cormier, Russel A.,Posey, Mary R.,Bell, William L.,Fonda, Harold N.,Connolly, John S.

, p. 4831 - 4844 (1989)

We have synthesized a porphyrin-anthraqu...

A simple method for efficient synthesis of tetrapyridyl-porphyrin using Adler method in acidic ionic liquids

Kitaoka, Satoshi,Nobuoka, Kaoru,Ihara, Keita,Ishikawa, Yuichi

, p. 26777 - 26782 (2014)

We investigated the preparation of tetra...

Synthesis and Spectroscopic Investigation of Directly Azobenzene Bridged Diporphyrins

Hombrecher, Hermann K.,Luedtke, Kerstin

, p. 9489 - 9494 (1993)

The synthesis of new directly azobenzene...

Donor-acceptor conjugates derived from cobalt porphyrin and fullerene via metal-ligand axial coordination: Formation and excited state charge separation

Subedi, Dili R.,Jang, Youngwoo,Ganesan, Ashwin,Schoellhorn, Sydney,Reid, Ryan,Verbeck, Guido F.,D'Souza, Francis

, p. 533 - 546 (2021/04/28)

Two types of cobalt porphyrins, viz., me...

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...

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...

14527-51-6 Process route

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

pyrrole

4-methyl-benzaldehyde
104-87-0

4-methyl-benzaldehyde

5,10,15,20-tetra(p-tolyl)porphyrin
14527-51-6

5,10,15,20-tetra(p-tolyl)porphyrin

Conditions
Conditions Yield
With propionic acid; In diethyl ether; at 60 ℃; for 0.5h;
70%
pyrrole; 4-methyl-benzaldehyde; With Tulsion-63 resin; Triethyl orthoacetate; In dichloromethane; at 20 ℃; for 16h;
With chloranil; In dichloromethane; for 2h; Heating;
68%
In propionic acid; for 5h; Reflux;
51%
With vanadium(V) oxychloride; In dichloromethane; for 1h; Ambient temperature; other reagents: TiCl4, VO(OEt)Cl2, VO(OiPr)Cl2, Mn(OAc)3;
50%
In propionic acid; nitrobenzene; for 0.75h; Reflux;
45%
pyrrole; 4-methyl-benzaldehyde; In ethylbenzene; propionic acid; at 159.6 ℃; for 0.166667h; under 1596.11 Torr; Large scale; Green chemistry;
With oxygen; In ethylbenzene; propionic acid; for 0.166667h; Large scale; Green chemistry;
42.2%
pyrrole; 4-methyl-benzaldehyde; With propionic acid; In ethylbenzene; at 159.6 ℃; for 0.166667h; under 1596.11 Torr;
With oxygen; In ethylbenzene; for 0.166667h; Reflux;
41.3%
With air; chloroacetic acid; In xylene; for 1.5h; Heating;
39%
With propionic acid; propionic acid anhydride;
35%
With propionic acid; for 2h; Reflux;
33.4%
4-methyl-benzaldehyde; With benzoic acid; at 200 ℃; for 0.0833333h; under 2736.18 Torr;
pyrrole; at 200 ℃; for 0.333333h;
30%
With boron trifluoride diethyl etherate; In dichloromethane; for 1h; Heating;
27%
pyrrole; 4-methyl-benzaldehyde; With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 0.5h;
With selenium(IV) oxide; In dichloromethane; for 1h;
23%
With propionic acid; at 120 ℃; for 1h; Reagent/catalyst;
21%
at 200 ℃; for 0.25h;
20%
In propionic acid; for 0.5h; Heating;
19.1%
pyrrole; 4-methyl-benzaldehyde; With trifluoroacetic acid; In dichloromethane; for 72h; Reflux;
With triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; at 20 ℃; for 1h;
8%
With propionic acid; In nitrobenzene; at 120 ℃; for 1h;
pyrrole; 4-methyl-benzaldehyde; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane;
39 % Spectr.
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;
With trifluoroacetic acid; In xylene; for 1.5h; Heating;
With trifluoroacetic acid; In dichloromethane; water; for 2h;
In propionic acid; Heating;
With propionic acid; Heating;
With propionic acid; for 2h; Reflux;
In propionic acid; Reflux;
With propionic acid; for 12h; Reflux;
In propionic acid; for 0.5h; Reflux;
With propionic acid; for 0.5h; Reflux;
With propionic acid; for 0.5h; Reflux;
With hydrogenchloride; In methanol; water; for 1h; Reflux; Inert atmosphere;
With propionic acid; for 1h; Reflux;
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; at 141 ℃; for 0.5h;
5,10,15,20-Tetra-p-tolyl-porphyrinogene

5,10,15,20-Tetra-p-tolyl-porphyrinogene

5,10,15,20-tetra(p-tolyl)porphyrin
14527-51-6

5,10,15,20-tetra(p-tolyl)porphyrin

Conditions
Conditions Yield
With chloranil; In tetrahydrofuran; water; Yield given;
With oxygen; 2,3-dicyano-5,6-dichloro-p-benzoquinone; iron(II) phthalocyanine μ-oxo dimer; In dichloromethane; for 2h;
660 mg
With air; In dichloromethane; at 39 ℃; for 4h;
With air; In dichloromethane; at 39 ℃;
With air; In dichloromethane; at 39 ℃; for 3h;
for 1.5h; 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;

14527-51-6 Upstream products

  • 109-97-7
    109-97-7

    pyrrole

  • 104-87-0
    104-87-0

    4-methyl-benzaldehyde

  • 121-32-4
    121-32-4

    4-hydroxy-3-ethoxybenzaldehyde

  • 42454-06-8
    42454-06-8

    2-nitro-5-hydroxybenzaldehyde

14527-51-6 Downstream products

  • 110934-98-0
    110934-98-0

    Dimethoxo<5,10,15,20-tetrakis(4-methylphenyl)porphyrinato>silicium(IV)

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