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| | 6-Hydroxy-5-nitronicotinic acid Basic information |
| | 6-Hydroxy-5-nitronicotinic acid Chemical Properties |
| Melting point | 269-271 | | Boiling point | 363.6±42.0 °C(Predicted) | | density | 1.70±0.1 g/cm3(Predicted) | | storage temp. | Inert atmosphere,Room Temperature | | pka | 3.09±0.50(Predicted) | | form | powder to crystal | | color | Light yellow to Yellow | | BRN | 177986 | | InChI | InChI=1S/C6H4N2O5/c9-5-4(8(12)13)1-3(2-7-5)6(10)11/h1-2H,(H,7,9)(H,10,11) | | InChIKey | VJMXJGVEVASJOD-UHFFFAOYSA-N | | SMILES | C1NC(=O)C([N+]([O-])=O)=CC=1C(O)=O | | CAS DataBase Reference | 6635-31-0(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37 | | Safety Statements | 26 | | WGK Germany | 3 | | Hazard Note | Irritant/Keep Cold | | HazardClass | IRRITANT | | HS Code | 2933399990 | | Storage Class | 13 - Non Combustible Solids | | Hazard Classifications | Eye Irrit. 2
STOT SE 3 |
| | 6-Hydroxy-5-nitronicotinic acid Usage And Synthesis |
| Uses |
6-Hydroxy-5-nitronicotinic acid is mainly used as an antibacterial agent and pharmaceutical intermediate.
| | Application | 6-Hydroxy-5-nitronicotinic acid serves as a multifunctional building block in medicinal and agrochemical synthesis: it acts as an antimicrobial agent, a pharmaceutical intermediate for vitamin B3 derivatives and other bio-actives, and a lead compound for antitumor, anti-inflammatory, antifungal and antiviral drug discovery. | | Chemical Reactivity | 6-Hydroxy-5-nitronicotinic acid is stable under proper conditions, it reacts with oxidizing agents.
| | Synthesis | 6-Hydroxy-5-nitronicotinic acid is synthesised using 6-Hydroxynicotinic acid as a raw material by chemical reaction. The specific synthesis steps are as follows:
6-Hydroxynicotinic acid 2 (25.0 g, 180 mmol) was dissolved in HNO3 fuming (1.52) (95 mL) and stirred at 50 oC for 18 h. After the solution was cooled to room temperature, the mixture was concentrated, and then co-evaporated with water, followed by the addition of MeOH to afford a brown precipitate. The precipitate was filtered and washed with 50 mL of cold MeOH twice. After drying under reduced pressure, a brown color product 3 was obtained; yield: 9.67 g (29percent); 1H NMR (300 MHz, CD3OD) 8.44 (d, J = 2.6 Hz, 1H), 8.85 (d, J = 2.6 Hz, 1H) ; HRMS (ES+): m/z 185.0194 (M+H+) (calcd for C6H5N2O5: 185.0198).
 | | References | [1] Tetrahedron Letters, 1999, vol. 40, # 12, p. 2227 - 2230
[2] Tetrahedron Letters, 2012, vol. 53, # 5, p. 535 - 538
[3] Patent: WO2016/138335, 2016, A1. Location in patent: Paragraph 00372
[4] Journal of the American Chemical Society, 1956, vol. 78, p. 423
[5] Journal of the Chemical Society, 1951, p. 2590,2593 |
| | 6-Hydroxy-5-nitronicotinic acid Preparation Products And Raw materials |
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