22112-80-7 Usage
General Description
4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis(2-methoxyphenol) is a chemical compound that belongs to the family of porphyrins. It is a tetrapyrrole macrocyclic compound that consists of four pyrrole rings connected by methine bridges. This chemical is a tetrakis(2-methoxyphenol) derivative of porphyrin, which means it has four 2-methoxyphenol groups attached to the porphyrin core. Porphyrins play a crucial role in biological functions, such as serving as the active component of hemoglobin, myoglobin, and many enzymes. The 2-methoxyphenol groups attached to this porphyrin molecule may confer specific properties or functions, making it potentially useful in various applications, such as in medical diagnostics, photodynamic therapy, or as a building block for designing new materials with specific properties. Further research and testing may reveal additional potential uses and applications for this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 22112-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,1 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22112-80:
(7*2)+(6*2)+(5*1)+(4*1)+(3*2)+(2*8)+(1*0)=57
57 % 10 = 7
So 22112-80-7 is a valid CAS Registry Number.
22112-80-7Relevant articles and documents
Supercapacitive hybrid materials from the thermolysis of porous coordination nanorods based on a catechol porphyrin
Jin, Shangbin,Hill, Jonathan P.,Ji, Qingmin,Shrestha, Lok Kumar,Ariga, Katsuhiko
, p. 5737 - 5744 (2016)
Synthesis of a series of porous coordination polymers with nanorod morphology constructed from a catechol-substituted porphyrin[meso-tetrakis(3,4-dihydroxyphenyl)porphyrin] is reported. While the coordination polymers had moderate surface areas (100-400 m
Synthesis and characterization of free base and metal porphyrins and their interaction with CdTe QDs
Jagadeeswari,Paramaguru,Renganathan
, p. 104 - 112 (2014)
Free base porphyrins and metalloporphyrins with different number of methoxy groups were synthesized to investigate the consequence of methoxy groups in the porphyrins on interaction with quantum dots through steady state, time resolved and transient absor
One-flask synthesis of porphyrin metal complexes
Manda, Amaravathi,Maradolla, Mohan Babu,Garimella, Chandramouli,Lingamallu, Giribabu
, p. 390 - 391 (2007)
One-flask synthesis of metallo porphyrins by condensation of aromatic aldehydes with pyrrole in refluxing propionic acid in presence of corresponding metal acetates is described. The yields are better when compared to Rothemund and Adler-Longo methods.
