| Identification | Back Directory | [Name]
5-FLUORO-1H-INDAZOLE-3-CARBALDEHYDE | [CAS]
485841-48-3 | [Synonyms]
5-FLUORO INDAZOLE-3-CARBOXALDEHYDE 5-FLUORO-1H-INDAZOLE-3-CARBALDEHYDE 5-fluoro-1H-Indazole-3-carboxaldehyde 5-fluoro-2H-indazole-3-carboxaldehyde 5-FLUORO-3-(1H)INDAZOLE CARBOXALDEHYDE 5-Fluoro-3-(1H)indazolecarboxyaldehyde 1H-Indazole-3-carboxaldehyde, 5-fluoro- 1H-Indazole-3-carboxaldehyde,5-fluoro-(9CI) | [Molecular Formula]
C8H5FN2O | [MDL Number]
MFCD06739142 | [MOL File]
485841-48-3.mol | [Molecular Weight]
164.14 |
| Hazard Information | Back Directory | [Uses]
5-fluoro-1H-indazole-3-carbaldehyde is used as a key intermediate in the synthesis of a variety of polyfunctionalized 3-substituted indazoles. | [Synthesis]
Step 3: Manganese dioxide (1.12 g, 12.9 mmol) was added to a solution of (5-fluoro-1H-indazol-3-yl)methanol (0.215 g, 1.29 mmol) in ethyl acetate (10 mL) at room temperature. The reaction mixture was stirred overnight and filtered through diatomaceous earth. The filtrate was concentrated and the resulting residue was purified by silica gel column chromatography (eluent: chloroform/methanol) to afford 5-fluoro-1H-indazole-3-carbaldehyde (0.150 g, 70% yield). The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 7.41 (ddd, J = 2.2,8.8,9.5 Hz, 1H), 7.75-7.81 (m, 2H), 10.18 (s, 1H), 14.32 (br s, 1H). | [References]
[1] Patent: EP2565192, 2013, A1. Location in patent: Paragraph 0352 |
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