Basic information Safety Supplier Related

1H-Indazole, 4-broMo-7-fluoro-

Basic information Safety Supplier Related

1H-Indazole, 4-broMo-7-fluoro- Basic information

Product Name:
1H-Indazole, 4-broMo-7-fluoro-
Synonyms:
  • 4-Bromo-7-fluoro-1H-indazole 96+%
  • 4-BroMo-7-fluoro-1H-indazole
  • 1H-Indazole, 4-broMo-7-fluoro-
  • 4-Bromo-7-fluoroindazole
  • 4-Bromo-7-fluoro-1H-indazole - [B17043]
CAS:
1186334-63-3
MF:
C7H4BrFN2
MW:
215.02
Mol File:
1186334-63-3.mol
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1H-Indazole, 4-broMo-7-fluoro- Chemical Properties

Boiling point:
330.3±22.0 °C(Predicted)
Density 
1.861±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
10.88±0.40(Predicted)
form 
solid
color 
White
InChI
InChI=1S/C7H4BrFN2/c8-5-1-2-6(9)7-4(5)3-10-11-7/h1-3H,(H,10,11)
InChIKey
ZDXVNDLMTIOXRC-UHFFFAOYSA-N
SMILES
N1C2=C(C(Br)=CC=C2F)C=N1
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Safety Information

RIDADR 
UN2811
HS Code 
2933998090
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1H-Indazole, 4-broMo-7-fluoro- Usage And Synthesis

Synthesis

360576-04-1

1186334-63-3

Step 2: Synthesis of 4-bromo-7-fluoro-1H-indazole; 6-bromo-2,3-difluorobenzaldehyde (11.2 g) was dissolved in dimethoxyethane (51 mL). To this solution anhydrous hydrazine (51 mL) was slowly added, followed by heating the reaction mixture to reflux for 2.5 hours. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the solvent dimethoxyethane was evaporated by rotary evaporator. The remaining reaction mixture was cooled in an ice bath followed by addition of ice-water mixture. The precipitated white solid was collected by filtration and washed with cold water. The resulting solid was dissolved in dichloromethane, warmed and filtered. The filtrate was concentrated to dryness, dissolved again in dichloromethane, warmed up and filtered. 4-Bromo-7-fluoro-1H-indazole (6.19 g, white solid) was finally obtained in 32% yield. Mass spectral (MS) data: 215.0, 217.0 [M + H].

References

[1] Patent: WO2009/108838, 2009, A1. Location in patent: Page/Page column 118

1H-Indazole, 4-broMo-7-fluoro-Supplier

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