Basic information Safety Supplier Related

4-Hydroxymethyl-1H-indazole

Basic information Safety Supplier Related

4-Hydroxymethyl-1H-indazole Basic information

Product Name:
4-Hydroxymethyl-1H-indazole
Synonyms:
  • 4-Hydroxymethyl-1H-indazole
  • 1H-INDAZOLE-4-METHANOL
  • (1H-indazol-4-yl)methanol
  • (1H-Indazol-4-yl)
CAS:
709608-85-5
MF:
C8H8N2O
MW:
148.16
Product Categories:
  • Building Blocks
  • Indazole
Mol File:
709608-85-5.mol
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4-Hydroxymethyl-1H-indazole Chemical Properties

Boiling point:
380.3±17.0 °C(Predicted)
Density 
1.360±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
13.92±0.40(Predicted)
color 
Grey to beige to brown
CAS DataBase Reference
709608-85-5
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Safety Information

HS Code 
2933998090
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4-Hydroxymethyl-1H-indazole Usage And Synthesis

Synthesis

192945-49-6

709608-85-5

General procedure for the synthesis of 4-(hydroxymethyl)-1H-indazole from methyl indazole-4-carboxylate: synthesis of (1H-indazol-4-yl)-methanol (18b): the ester obtained above (40 mg, 0.23 mmol) was dissolved in 1 mL of tetrahydrofuran (THF) and the solution was cooled to 0°C. A THF solution (1.0 M, 2.3 mL, 2.3 mmol) of diisobutylaluminum hydride (DIBAL) was added slowly and dropwise. The addition of DIBAL was continued until the feedstock was completely consumed. Upon completion of the reaction, the reaction was quenched with saturated sodium potassium tartrate solution and gradually warmed to room temperature. The reaction mixture was extracted using ethyl acetate. The organic phases were combined and dried with anhydrous magnesium sulfate (MgSO4). Subsequently, the solvent was removed by reduced pressure distillation and the residue was purified by column chromatography (75% ethyl acetate/hexane). The final target product (20 mg, 60% yield) was obtained as a white solid. Mass spectrometry (electrospray ionization) analysis showed that the theoretical value of M + H = 149.1 and the measured value = 149.1.

References

[1] Patent: WO2007/51062, 2007, A2. Location in patent: Page/Page column 126-127

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