Basic information Safety Supplier Related

7-Chloro-1H-indole-3-carbaldehyde

Basic information Safety Supplier Related

7-Chloro-1H-indole-3-carbaldehyde Basic information

Product Name:
7-Chloro-1H-indole-3-carbaldehyde
Synonyms:
  • 7-CHLORO-3-FORMYLINDOLE
  • 7-Chloro-3-indolecarboxaldehyde
  • 1H-Indole-3-carboxaldehyde, 7-chloro-
  • 7-Chloro-3-formyl-1H-indole
  • 7-Chloroindole-3-carbaldehyde
  • 7-CHLORO-1H-INDOLE-3-CARBALDEHYDE
  • 7-chloro-3-formylindole, CAS 1008-07-7
  • 7-Chloro-1H-indol-3-carbaldehyde
CAS:
1008-07-7
MF:
C9H6ClNO
MW:
179.6
Mol File:
1008-07-7.mol
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7-Chloro-1H-indole-3-carbaldehyde Chemical Properties

Melting point:
181-182 °C(Solv: ethyl acetate (141-78-6))
Boiling point:
373.4±22.0 °C(Predicted)
Density 
1.431±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
13.92±0.30(Predicted)
Appearance
White to yellow Solid
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Safety Information

HS Code 
2933998090
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7-Chloro-1H-indole-3-carbaldehyde Usage And Synthesis

Synthesis

53924-05-3

1008-07-7

The general procedure for the synthesis of 7-chloro-1H-indole-3-aldehyde from 7-chloro-1H-indole was as follows: phosphoryl chloride (0.66 mL, 7 mmol) was slowly added dropwise to anhydrous DMF (5 mL) at 0 °C and under argon protection. Subsequently, a solution of 7-chloro-1H-indole (1 g, 6.6 mmol) dissolved in anhydrous DMF (15 mL) was added dropwise to the above mixture at room temperature. The reaction mixture was stirred continuously for 2 hours at room temperature. After completion of the reaction, the mixture was slowly poured into a mixture of ice water and saturated NaHCO3 solution and extracted with ethyl acetate. The organic phases were combined, washed with saturated NaCl solution (10 mL x 3), dried over anhydrous MgSO4, filtered and concentrated to give 990 mg of the target product 7-chloro-1H-indole-3-aldehyde as a yellow-orange solid in 83% yield.

References

[1] Patent: US2005/119260, 2005, A1. Location in patent: Page/Page column 36

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