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| 2,2-bipyridine-6-carboxylic acid Basic information | | Uses |
| Product Name: | 2,2-bipyridine-6-carboxylic acid | | Synonyms: | 2,2-bipyridine-6-carboxylic acid;6-pyridin-2-ylpyridine-2-carboxylic Acid;2-Amino-4-(4-fluorbenzylamino)-6-ethoxycarbonylaminobenzene;5-Pyrimidinecarboxylicacid,4-chloro-8-(methylthio)-;N-Boc-piperidine-7-carbaldehyde;1H-Isoindole-1,3(2H)-dione,2-[2-(3,4-dihydro-2,2,4-trimethyl-1(2H)-quinolinyl)-6-oxoethyl]-;DK7358 | | CAS: | 4392-87-4 | | MF: | C11H8N2O2 | | MW: | 200.19 | | EINECS: | | Product Categories: | Carboxylic Acids;Pyridines;Carboxylic Acids | | Mol File: | 4392-87-4.mol |
| 2,2-bipyridine-6-carboxylic acid Chemical Properties |
| Melting point | 210-220 °C (decomp) | | Boiling point | 427.7±35.0 °C(Predicted) | | density | 1.302±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | form | powder or crystals | | pka | 2.93±0.10(Predicted) |
| 2,2-bipyridine-6-carboxylic acid Usage And Synthesis |
| Uses | 2,2'-Bipyridine-6-carboxylic Acid is a useful research chemical compound. | | Uses | Developed in the Engle lab, this 2,2′-bipyridylamide (PPA) is a pincer-like, removable tridentate directing group that stabilizes 6-membered palladacycles for olefin functionalization. Together with similar ligand PAQ (901250), researchers demonstrated regioselective remote hydrocarbofunctionalization of alkene-containing substrate classes (e.g. 4-pentenoic acids, allylic alcohols, homoallyl amines, bis-homoallylamines) using Pd(II) catalysis. |
| 2,2-bipyridine-6-carboxylic acid Preparation Products And Raw materials |
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