Names | |
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Preferred IUPAC name
2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline | |
Other names
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Identifiers | |
CAS Number
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3D model (JSmol)
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ChEMBL |
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ChemSpider |
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ECHA InfoCard | 100.022.945 |
EC Number |
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PubChem CID
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UNII |
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CompTox Dashboard (EPA)
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InChI
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SMILES
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Properties | |
Chemical formula
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C26H20N2 |
Molar mass | 360.460 g·mol−1 |
Appearance | Pale yellow solid |
Melting point | 283 °C (541 °F; 556 K) |
Solubility in water
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organic solvents |
Hazards | |
GHS labelling: | |
Pictograms
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Signal word
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Warning |
Hazard statements
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H302, H413 |
Precautionary statements
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P264, P270, P273, P301+P312, P330, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Bathocuproine is a derivative of 1,10-phenanthroline with two methyl groups and two phenyl groups in the 2,9 and 4,7 positions, respectively. Like 1,10-phenanthroline, bathocuproine is a bidentate chelating ligand. The two methyl groups flank the nitrogen centers, such that bathocuproine is a bulky ligand. This compound, first prepared by Case and Brennan in the early 1950s [1][2] is a pale yellow solid that is soluble in polar organic solvents.[3]
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