What is the PORPHINE?

PORPHINE is , while it's Molecular Formula is C20H14N4. Used in Pharmaceutical Industry: Porphine serves as a crucial component in the development of pharmaceutical compounds, particularly in the synthesis of porphyrin-based drugs. Its unique structure and properties make it an ideal candidate for the creation of novel therapeutic agents with potential applications in various medical fields. Used in Chemical Industry: In the chemical industry, Porphine is utilized as a key building block for the synthesis of a variety of porphyrin complexes. These complexes find applications in areas such as catalysis, where they can act as catalysts or catalyst supports, and in the development of new materials with unique properties. Used in Material Science: Porphine's planar structure and chemical versatility make it a valuable component in the field of material science. It is used in the design and synthesis of advanced materials with tailored properties, such as???? (photoelectric materials), which have potential applications in solar cells, light-emitting diodes (LEDs), and other optoelectronic devices. Used in Environmental Applications: Porphine and its derivatives have been explored for their potential use in environmental remediation, particularly in the removal of pollutants from water and air. Their ability to bind and degrade contaminants makes them promising candidates for the development of new environmental technologies. Used in Analytical Chemistry: Porphine's unique optical and electronic properties make it a valuable tool in analytical chemistry. It can be employed as a chromophore in the development of new spectroscopic methods for the detection and analysis of various compounds and materials.

What is the CAS number for PORPHINE?

The CAS number of PORPHINE is 101-60-0.

What is PORPHINE (101-60-0) used for?

Porphine (also called porphin) is a planar aromatic heterocyclic compound with a 12-carbon outside ring and four embedded pyrrole rings. It is a dark red crystalline solid that is soluble in some polar solvents such as pyridine and dioxane. It can be heated to 360 oC without melting. Porphine is the parent compound of a family of biologically and chemically relevant compounds called porphyrins. The potential of these compounds is enormous and it would be advantageous to use the porphine (porphyrin) unit as a building block for the synthesis of diverse porphyrin complexes with a wide range of applications.InChI:InChI=1/C20H14N4/c1-2-14-10-16-5-6-18(23-16)12-20-8-7-19(24-20)11-17-4-3-15(22-17)9-13(1)21-14/h1-12,21,24H/b13-9-,14-10-,15-9-,16-10-,17-11-,18-12-,19-11-,20-12-

What is the PORPHINE?

PORPHINE is , while it's Molecular Formula is C20H14N4. Used in Pharmaceutical Industry: Porphine serves as a crucial component in the development of pharmaceutical compounds, particularly in the synthesis of porphyrin-based drugs. Its unique structure and properties make it an ideal candidate for the creation of novel therapeutic agents with potential applications in various medical fields. Used in Chemical Industry: In the chemical industry, Porphine is utilized as a key building block for the synthesis of a variety of porphyrin complexes. These complexes find applications in areas such as catalysis, where they can act as catalysts or catalyst supports, and in the development of new materials with unique properties. Used in Material Science: Porphine's planar structure and chemical versatility make it a valuable component in the field of material science. It is used in the design and synthesis of advanced materials with tailored properties, such as光电材料 (photoelectric materials), which have potential applications in solar cells, light-emitting diodes (LEDs), and other optoelectronic devices. Used in Environmental Applications: Porphine and its derivatives have been explored for their potential use in environmental remediation, particularly in the removal of pollutants from water and air. Their ability to bind and degrade contaminants makes them promising candidates for the development of new environmental technologies. Used in Analytical Chemistry: Porphine's unique optical and electronic properties make it a valuable tool in analytical chemistry. It can be employed as a chromophore in the development of new spectroscopic methods for the detection and analysis of various compounds and materials.

What is the CAS number for PORPHINE?

The CAS number of PORPHINE is 101-60-0.

What is PORPHINE (101-60-0) used for?

Porphine (also called porphin) is a planar aromatic heterocyclic compound with a 12-carbon outside ring and four embedded pyrrole rings. It is a dark red crystalline solid that is soluble in some polar solvents such as pyridine and dioxane. It can be heated to 360 oC without melting. Porphine is the parent compound of a family of biologically and chemically relevant compounds called porphyrins. The potential of these compounds is enormous and it would be advantageous to use the porphine (porphyrin) unit as a building block for the synthesis of diverse porphyrin complexes with a wide range of applications.InChI:InChI=1/C20H14N4/c1-2-14-10-16-5-6-18(23-16)12-20-8-7-19(24-20)11-17-4-3-15(22-17)9-13(1)21-14/h1-12,21,24H/b13-9-,14-10-,15-9-,16-10-,17-11-,18-12-,19-11-,20-12-

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PORPHINE

CAS: 101-60-0
Purity: 99%
Cosmetics Grade PORPHINE 101-60-0 For Sale with Good Price

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Product Detail

Cosmetics Grade PORPHINE 101-60-0 For Sale with Good Price

Molecular Formula: C20H14N4
Molecular Weight: 310.358
Vapor Pressure: 0mmHg at 25°C
Melting Point: 360°C
Refractive Index: 1.72
Boiling Point: 804.4 °C at 760 mmHg
Flash Point: 377.479 °C
PSA： 56.30000
Density: 1.353 g/cm³
LogP: 1.19220

PORPHINE(Cas 101-60-0) Usage

History

Porphine was first prepared by German chemists Hans Fischer and Wilhelm Gleim in 1935. It is the parent structure of a large family of natural compounds called porphyrins, many of which are essential to life. Fischer was a 1930 Nobel Prize winner for his research on two porphyrins, heme (a constituent of hemoglobin) and chlorophyll. These porphyrins, like many others, contain a metal atom coordinated to the four nitrogen atoms.

Chemical Synthesis

Porphine is the simplest porphyrin and represents the core macrocycle of naturally occurring and synthetic porphyrins. Low yields and expense, however, make the synthesis of porphine on a large scale impractical. Another challenge synthetic chemist's faced was the high insolubility of porphine. The apolar tetrapyrrolic ring structure of porphine means it is poorly soluble in most organic solvents and hardly water soluble. As a result of this almost all current chemical studies with porphyrins use the better soluble meso tetrasubstituted 2 or β-octasubstituted porphyrins.

InChI:InChI=1/C20H14N4/c1-2-14-10-16-5-6-18(23-16)12-20-8-7-19(24-20)11-17-4-3-15(22-17)9-13(1)21-14/h1-12,21,24H/b13-9-,14-10-,15-9-,16-10-,17-11-,18-12-,19-11-,20-12-

101-60-0 Relevant articles

Convenient synthesis of porphine from β-tetra(tert-butyl)porphyrin

Neya, Saburo,Quan, Jingshun,Hoshino, Tyuji,Hata, Masayuki,Funasaki, Noriaki

, p. 8629 - 8630 (2004)

β-Tetra(tert-butyl)porphyrin was prepare...

Protonation salt derivative with heavy-atom effect on phthalocyanine for enhanced in vitro photodynamic therapy

Chen, Xianglan,Li, Yejing,Wang, Ao,Zhou, Lin,Lu, Shan,Zhou, Jiahong,Lin, Yun,Wei, Shaohua

, p. 93 - 104 (2015)

In order to improve water-solubility and...

Inducing Open-Shell Character in Porphyrins through Surface-Assisted Phenalenyl π-Extension

Bottari, Giovanni,Fasel, Roman,Lorente, Nicolas,Mateo, Luis M.,Robles, Roberto,Ruffieux, Pascal,Sun, Qiang,Torres, Tomás

, p. 18109 - 18117 (2020)

Organic open-shell compounds are extraor...

-

Hodgson,Baker

, p. 29,30,31 (1967)

meso-tetra(tert-butyl)porphyrin as a precursor of porphine

Neya, Saburo,Funasaki, Noriaki

, p. 1057 - 1058 (2002)

Treatment of meso-tetra(tert-butyl)porph...

Direct synthesis of magnesium porphine via 1-formyldipyrromethane

Dogutan, Dilek Kiper,Ptaszek, Marcin,Lindsey, Jonathan S.

, p. 5008 - 5011 (2007)

(Chemical Equation Presented) The reacti...

A facile route to tripyrrane from 2,5-bis(hydroxymethyl)pyrrole and the improved synthesis of porphine by the '3+1' approach

Taniguchi, Shozo,Hasegawa, Hikaru,Nishimura, Masato,Takahashi, Masahiko

, p. 73 - 74 (1999)

The treatment of 2,5-bis(hydroxymethyl)p...

Porphine and pyrrole-substituted porphyrin from cyclocondensation of tripyrrane with mono-substituted pyrroles

Saltsman, Irena,Goldberg, Israel,Balasz, Yael,Gross, Zeev

, p. 239 - 244 (2007)

The condensation of non-substituted trip...

A novel and efficient synthesis of porphine

Neya, Saburo,Quan, Jingshun,Hata, Masayuki,Hoshino, Tyuji,Funasaki, Noriaki

, p. 8731 - 8732 (2006)

meso-Tetra(n-hexyloxycarbonyl)porphyrin ...

The facile synthesis of 5-formylporphyrin

Liu, Peng Peng,Feng, Ya Qing,Gu, Cheng Zhi,Meng, Shu Xian,Zhang, Bao

, p. 505 - 508 (2012)

A facile synthetic route of 5-formylporp...

High-Resolution Solid-State 13C NMR Spectra of Porphine and 5,10,15,20-Tetraalkylporphyrins: Implications for the N-H Tautomerization Process

Frydman, Lucio,Olivieri, Alejandro C.,Diaz, Luis E.,Frydman, Benjamin,Morin, Frederick G.,et al.

, p. 336 - 342 (1988)

The solid-state high-resolution 13C nucl...

-

Rothemund

, (1939)

Concerning the Crystal Structure of Porphine: A Proton Pulsed and 13C CPMAS NMR Study

Frydman, Lucio,Olivieri, Alejandro C.,Diaz, Luis E.,Frydman, Benjamin,Kustanovich, Irina,Vega, Shimon

, p. 7001 - 7005 (1989)

Solid-state NMR techniques were employed...

-

Dicker et al.

, p. 560 (1967)

-

Krol

, p. 2065 (1959)

The influence of protonation on the structure and spectral properties of porphine: UV-vis, 1H NMR and: Ab initio studies

Zakavi, Saeed,Omidyan, Reza,Talebzadeh, Sadegh

, p. 82219 - 82226 (2016/09/09)

In this study, protonation of porphine (...

Soluble porphyrin polymers

-

Page/Page column, (2015/07/15)

Porphyrin polymers of Structure 1, where...

101-60-0 Process route

: 4-(4-((tritylamino)methyl)phenoxy)phthalonitrile

: 101-60-0
porphyrin

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In n-heptan1ol;	80%

: 27472-36-2
2-hydroxymethylpyrrole

: 101-60-0
porphyrin

Conditions

Conditions	Yield
With dipotassium peroxodisulfate; magnesium acetate;
With acetic acid; In xylene; at 110 - 115 ℃;
With acetic acid; In xylene; at 110 - 115 ℃; Heating;
Multi-step reaction with 2 steps 1: aq. sodium dodecyl sulfate, HCl / 0.17 h 2: 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / H₂O; tetrahydrofuran / 0.5 h With hydrogenchloride; sodium dodecyl-sulfate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; water;