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J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788 |
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jkinfo@jkchemical.com |
Products Intro: |
Product Name:5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin CAS:119730-06-2 Purity:90.0%(LC) Package:100MG,1G
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Company Name: |
Meryer (Shanghai) Chemical Technology Co., Ltd.
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021-61259108 18621169109 |
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market03@meryer.com |
Products Intro: |
Product Name:5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin CAS:119730-06-2 Purity:>90.0%(LC) Package:100Mg;1g Remarks:M1338
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| 5-(4-METHOXYCARBONYLPHENYL)-10,15,20-TRIPHENYL-21H,23H-PORPHINE Basic information |
Product Name: | 5-(4-METHOXYCARBONYLPHENYL)-10,15,20-TRIPHENYL-21H,23H-PORPHINE | Synonyms: | 5-(4-Carbomethoxyphenyl)-10,15,20-triphenylporphyrin
5-(4-Methoxycarbonylphenyl)-10,15,20-triphenyl-21H,23H-porphine;Benzoic acid, 4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)-, methyl ester;RARECHEM AS SA 0020;5-(4-Methoxycarbonylphenyl)-10,15,20-triphenyl-21H;5-(4-Carbomethoxyphenyl)-10,15,20-triphenylporphyrin;5-(4-CARBOMETHOXYPHENYL)-10,15,20-TRIPHENYL-21H,23H-PORPHINE;5-(4-METHOXYCARBONYLPHENYL)-10,15,20-TRIPHENYL-21H,23H-PORPHINE;5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin | CAS: | 119730-06-2 | MF: | C46H32N4O2 | MW: | 672.77 | EINECS: | | Product Categories: | Absolute Configuration Determination (Exciton Chirality CD Method);Analytical Chemistry;Biochemistry;Enantiomer Excess & Absolute Configuration Determination;Exciton Chirality CD Method (for Hydroxyl Groups);Porphyrins | Mol File: | 119730-06-2.mol | |
| 5-(4-METHOXYCARBONYLPHENYL)-10,15,20-TRIPHENYL-21H,23H-PORPHINE Chemical Properties |
Melting point | 268-270 °C(Solv: chloroform (67-66-3); methanol (67-56-1)) | density | 1.273±0.06 g/cm3(Predicted) | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | form | powder to crystal | color | Dark red to Dark purple to Dark blue |
| 5-(4-METHOXYCARBONYLPHENYL)-10,15,20-TRIPHENYL-21H,23H-PORPHINE Usage And Synthesis |
Uses | 5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin (CAS# 119730-06-2) is a porphyrin derivative used in the preparation of metal-free photo-organocatalysts for enantioselective aerobic oxidation of β-dicarbonyl compounds, and in the preparation of luminous composites from layered inorganic-organic monolith contiguous neutral porphyrins. |
| 5-(4-METHOXYCARBONYLPHENYL)-10,15,20-TRIPHENYL-21H,23H-PORPHINE Preparation Products And Raw materials |
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