Basic information Safety Supplier Related

5,7-Difluoroindole

Basic information Safety Supplier Related

5,7-Difluoroindole Basic information

Product Name:
5,7-Difluoroindole
Synonyms:
  • 5,7-DIFLUOROINDOLE
  • 5,7-difluoroinde
  • 1H-Indole,5,7-difluoro-(9CI)
  • 5,7-Difluoro-1H-Indole
  • 1H-Indole, 5,7-difluoro-
  • SWF-101
  • SW-101
  • 5,8-Difluoroindole
CAS:
301856-25-7
MF:
C8H5F2N
MW:
153.13
Product Categories:
  • HALIDE
  • INDOLE
  • Indoles and derivatives
  • pharmacetical
  • Indoles
Mol File:
301856-25-7.mol
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5,7-Difluoroindole Chemical Properties

Boiling point:
253.2±20.0 °C(Predicted)
Density 
1.388±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
14.71±0.30(Predicted)
form 
liquid
color 
Light yellow
InChI
InChI=1S/C8H5F2N/c9-6-3-5-1-2-11-8(5)7(10)4-6/h1-4,11H
InChIKey
WZPOGQRJXZGSMH-UHFFFAOYSA-N
SMILES
N1C2=C(C=C(F)C=C2F)C=C1
CAS DataBase Reference
301856-25-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2933998090
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5,7-Difluoroindole Usage And Synthesis

Synthesis

500139-00-4

301856-25-7

Example 4: Synthesis of the intermediate 5,7-difluoro-1H-indole To a solution of ethanol (35 mL) containing NaOEt (1.83 g, 26.9 mmol), a solution of ethyl (2,4-difluoro-6-trimethylsilylethynylphenyl)carbamate (2 g, 6.73 mmol) in ethanol (10 mL) was slowly added. The reaction mixture was stirred at room temperature for 1 h (monitored by TLC until the disappearance of the feedstock), followed by refluxing for 1 h. The reaction was completed by cooling to room temperature. After completion of the reaction, it was cooled to room temperature and the reaction mixture was concentrated under vacuum. The residue was dissolved in ether (50 mL) and washed sequentially with dilute hydrochloric acid (3 x 25 mL) and saturated saline (3 x 25 mL). The organic layer was dried with anhydrous Na2SO4, filtered and concentrated in vacuum. Purification by silica gel fast column chromatography (eluent ratio 1:4 ethyl acetate:hexane) gave 770 mg of the title compound in 75% yield.

References

[1] Patent: WO2005/12291, 2005, A1. Location in patent: Page/Page column 63

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