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CAS RN: 28903-71-1 | Product Number: T1861

[5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II)


Purity: >96.0%(T)
Synonyms:
  • [5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphinato]cobalt(II)
Documents:
1G
$51.00
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5G
$175.00
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* The storage conditions are subject to change without notice.


Product Number T1861
Purity / Analysis Method >96.0%(T)
Molecular Formula / Molecular Weight C__4__8H__3__6CoN__4O__4 = 791.77  
Physical State (20 deg.C) Solid
CAS RN 28903-71-1
Reaxys Registry Number 1208624
PubChem Substance ID 87577584
MDL Number

MFCD00010724

Specifications
Appearance Dark red to Dark purple to Dark blue powder to crystal
Purity(Chelometric Titration) min. 96.0 %
Lambda max. 415.0 to 425.0 nm(THF)
Absorbance(E1%1cm) min. 2000(THF, 415.0 to 425.0 nm)
Properties (reference)
Maximum Absorption Wavelength 420(THF) nm
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H351 : Suspected of causing cancer.
Precautionary Statements P501 : Dispose of contents/ container to an approved waste disposal plant.
P202 : Do not handle until all safety precautions have been read and understood.
P201 : Obtain special instructions before use.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection.
P308 + P313 : IF exposed or concerned: Get medical advice/ attention.
P405 : Store locked up.
Related Laws:
Transport Information:
H.S.code* 2933.99-000
*This code is applied to the products when TCI exports from Japan and not for import in your country.
Application
The Co(II)-Porphyrin-catalyzed Aerobic Oxidative Coupling of Phenols

Typical Procedure:
[5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II) (0.2 mol%), phenol (1.0 mmol), Na2CO3 (1.0 mmol), MeOH (4.0 mL), and H2O (1.0 mL) are added to a 25 mL flame-dried Schlenk tube in air. The air is removed by vacuum, and O2 (1 atm) is introduced. The Schlenk tube is then sealed, and the resulting mixture is stirred at 60 °C under an atmosphere of oxygen (1 atm). After stirring for the time indicated, the mixture is cooled to room temperature, carefully acidified with dilute aqueous HCl, diluted with AcOEt (10 mL), filtered through a plug of silica gel, and washed with AcOEt (20–30 mL). The combined organic extract is dried with anhydrous MgSO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by column chromatography on silica gel to afford the desired product.

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