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| 2-Amino-3-hydroxypyridine Basic information |
| 2-Amino-3-hydroxypyridine Chemical Properties |
Melting point | 168-172 °C (lit.) | Boiling point | 206.4°C (rough estimate) | density | 1.2111 (rough estimate) | vapor pressure | 0.007-0.28Pa at 20-50℃ | refractive index | 1.4800 (estimate) | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | solubility | DMSO (Slightly), Methanol (Slightly) | pka | 5.15±0.10(Predicted) | form | Crystalline Powder | color | Grayish-beige to brownish | BRN | 109868 | InChIKey | BMTSZVZQNMNPCT-UHFFFAOYSA-N | LogP | -0.25 at 23℃ and pH7.02-7.04 | Surface tension | 72.6mN/m at 1.053g/L and 20℃ | CAS DataBase Reference | 16867-03-1(CAS DataBase Reference) | NIST Chemistry Reference | 2-Amino-3-hydroxypyridine(16867-03-1) |
| 2-Amino-3-hydroxypyridine Usage And Synthesis |
Chemical Properties | white to light yellow crystal powder | Uses | 2-Amino-3-hydroxypyridine was used as reagent in reaction of dimethyl acetylenedicarboxylate and triphenylphosphine to yield functionalized coumarins and 1,4-oxazines. | Synthesis Reference(s) | Journal of Heterocyclic Chemistry, 14, p. 203, 1977 DOI: 10.1002/jhet.5570140206 | General Description | 2-Amino-3-hydroxypyridine forms complexes with number of transition metals. It inhibits the corrosion of aluminium and copper in acidic solutions. It undergoes condensation with 2-hydroxy-1-naphthaldehyde and 2-hydroxybenzaldehyde to form Schiffs bases. It is useful in the preparation of clinical anti-inflammatory analgesics. |
| 2-Amino-3-hydroxypyridine Preparation Products And Raw materials |
Raw materials | 3-Hydroxypicolinic acid-->2-Amino-3-benzyloxypyridine-->3-HYDROXYPICOLINAMIDE-->2-FURAMIDE-->2-Amino-3-ethoxypyridine-->2-IODO-3-HYDROXYPYRIDINE-->3-Hydroxy-2-nitropyridine-->Hexamethylphosphoramide-->3-Nitro-2-pyridinol-->3-Hydroxypyridine | Preparation Products | 2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one-->3-(2-Chloroethyl)-6,7,8,9-tetrahydro-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one-->Paliperidone Impurity 4-->tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate-->2H-Pyrido[3,2-b][1,4]oxazin-3(4H)-one-->N,N-DiMethyl-4-(oxazolo[4,5-b]pyridin-2-yl)aniline-->3-[(3,4-DICHLOROBENZYL)OXY]PYRIDIN-2-AMINE |
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