2,6-Diphenylpyridine, 97%, Thermo Scientific Chemicals
2,6-Diphenylpyridine, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2,6-Diphenylpyridine, 97%, Thermo Scientific Chemicals

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Quantity:
25 g
5 g
Catalog number B25179.14
also known as B25179-14
Price (USD)/ Each
338.00
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Quantity:
25 g
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Price (USD)/ Each
338.00
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2,6-Diphenylpyridine, 97%, Thermo Scientific Chemicals
Catalog numberB25179.14
Price (USD)/ Each
338.00
-
Add to cart
Chemical Identifiers
CAS3558-69-8
IUPAC Name2,6-diphenylpyridine
Molecular FormulaC17H13N
InChI KeyPJUOHDQXFNPPRF-UHFFFAOYSA-N
SMILESC1=CC=C(C=C1)C1=CC=CC(=N1)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream
FormCrystals or powder or crystalline powder
Assay (GC)≥96.0%
Melting Point (clear melt)77.0-87.0?C
2,6-Diphenylpyridine is used as a tridentate [C?N?C] dianionic ligand in organogold(III) chemistry, an intermediate. It readily adds an electron from alkali metals in THF to give a radical anion which is a powerful reducing agent.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2,6-Diphenylpyridine is used as a tridentate [C∧N∧C] dianionic ligand in organogold(III) chemistry, an intermediate. It readily adds an electron from alkali metals in THF to give a radical anion which is a powerful reducing agent.

Solubility
Insoluble in water.

Notes
Store in a cool, dry place in tightly closed container. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Matthew Polson; Sandro Fracasso; Valerio Bertolasi; Marcella Ravaglia; and Franco Scandola. Iridium Cyclometalated Complexes with Axial Symmetry. Synthesis and Photophysical Properties of a trans-Biscyclometalated Complex Containing the Terdentate Ligand 2,6-Diphenylpyridine. Inorg. Chem. 2004, 43 (6), 1950-1956.
  2. Kar-Ho Wong; Kung-Kai Cheung; Michael Chi-Wang Chan; and Chi-Ming Che. Application of 2,6-Diphenylpyridine as a Tridentate [C∧N∧C] Dianionic Ligand in Organogold(III) Chemistry. Structural and Spectroscopic Properties of Mono- and Binuclear Transmetalated Gold(III) Complexes. Organometallics. 1998, 17 (16), 3505-3511.
  3. Readily adds an electron from alkali metals in THF to give a radical anion which is a powerful reducing agent: e.g. reacting with benzophenone to give the dianion which can be carbonated with CO2 to give benzilic acid: Bull. Soc. Chim. Fr., 1710 (1960).