Identification | Back Directory | [Name]
4-HYDROXYINDAZOLE | [CAS]
81382-45-8 | [Synonyms]
1H-Indazol-4-ol 4-HYDROXYINDAZOLE 1H-Indazol-4-ol ,97% 4-Hydroxy-1H-indazole 4-Hydroxyindazole HCl 4-HYDROXYL (1H)INDAZOLE 4-Hydroxyindazole hydrochloride 1,2-dihydroindazol-4-one hydrochloride | [EINECS(EC#)]
200-258-5 | [Molecular Formula]
C7H6N2O | [MDL Number]
MFCD06858736 | [MOL File]
81382-45-8.mol | [Molecular Weight]
134.14 |
Chemical Properties | Back Directory | [Melting point ]
177-178℃ | [Boiling point ]
366.5±15.0 °C(Predicted) | [density ]
1.434±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
8.76±0.40(Predicted) | [Appearance]
Light yellow to green yellow Solid |
Hazard Information | Back Directory | [Chemical Properties]
White to off-white solid | [Synthesis]
C. General procedure for the preparation of 4-hydroxyindazole from 4-aminoindazole: 4-aminoindazole (9.6 g, 0.072 mol) was dissolved in a glass reaction vessel containing 7.2 g of concentrated sulfuric acid in 75 mL of water. The mixture was transferred to a stainless steel autoclave, sealed and heated to 170°C for overnight reaction. Upon completion of the reaction, a large amount of black precipitate appeared in the reaction mixture. The reaction mixture was diluted with ethyl acetate and water and transferred to a dispensing funnel for distribution. The aqueous layer was extracted with ethyl acetate several times until 4-hydroxyindazole was completely transferred to the organic phase. The organic phases were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated to give a dark brown or black oil. The crude product was purified by silica gel column chromatography with an eluent of 50% ethyl acetate/hexane mixture to give 4-hydroxyindazole as an off-white solid (3.3 g, 33% yield). | [References]
[1] Patent: WO2004/39796, 2004, A1. Location in patent: Page/Page column 71-72 [2] Patent: US6534504, 2003, B1 [3] Patent: US6841563, 2005, B1. Location in patent: Page column 20 [4] Journal of Medicinal Chemistry, 2012, vol. 55, # 8, p. 3975 - 3991 [5] Journal of the Chemical Society, 1955, p. 2412,2419 |
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