| Weight | 202.007 g/mol |
|---|---|
| Formula | C6H4BrNO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
5-bromopyridine-2-carboxylic acid (30766-11-1)
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- Coordination geometry of monomeric, dimeric and polymeric organotin(IV) compounds constructed from 5-bromopyridine-2-carboxylic acid and mono-, di- or tri-organotin precursors (Journal of Molecular Structure, 2013)
- One-Pot Synthesis of Furo[3,4-b]pyridin-5(7H)-onesfrom 2-Bromopyridine-3-carboxylic Acid and Carbonyl Compounds (Synthesis, 2009)
- Tandem Palladium/CharcoalCopper(I) Iodide (Pd/CCuI) Catalyzed Sonogashira Coupling and Intramolecular Cyclization from 2Bromonicotinic Acid (=2Bromopyridine3carboxylic Acid) and Ethynylarenes to 4Azaphthalides (=Furo[3,4b]pyridin5(7H)ones) and 5Azaisocoumarins (=5HPyrano[4,3b]pyridin5ones) (Helvetica Chimica Acta, 2011)
- ChemInform Abstract: One-Pot Synthesis of Furo[3,4-b]pyridin-5(7H)-ones from 2-Bromopyridine-3-carboxylic Acid and Carbonyl Compounds. (ChemInform, 2010)
- ChemInform Abstract: Tandem Palladium/Charcoal-Copper(I) Iodide (Pd/CCuI) Catalyzed Sonogashira Coupling and Intramolecular Cyclization from 2-Bromonicotinic Acid (= 2-Bromopyridine-3-carboxylic Acid) and Ethynylarenes to 4-Azaphthalides (= Furo[3,4-b]pyridin-5(7H)-ones) and 5-Azaisocoumarins (= 5H-Pyrano[4,3-b]pyridin-5-ones). (ChemInform, 2012)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC(=NC=C1Br)C(=O)O
-
InChIKeyMNNQIBXLAHVDDL-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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