ChemicalBook--->CAS DataBase List--->854778-47-5

854778-47-5

854778-47-5 Structure

854778-47-5 Structure
IdentificationBack Directory
[Name]

1-ethyl-1H-indole-6-carbaldehyde
[CAS]

854778-47-5
[Synonyms]

Albb-004942
1-ethyl-1H-indole-6-carbaldehyde
1H-Indole-6-carboxaldehyde, 1-ethyl-
1-ethyl-1H-indole-6-carbaldehyde(SALTDATA: FREE)
[Molecular Formula]

C11H11NO
[MDL Number]

MFCD09455258
[MOL File]

854778-47-5.mol
[Molecular Weight]

173.21
Chemical PropertiesBack Directory
[Boiling point ]

327.7±15.0 °C(Predicted)
[density ]

1.08±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
Questions And AnswerBack Directory
[Uses]

1-Ethyl-1H-indole-6-carboxaldehyde is an aldehyde derivative that can be used as a biochemical reagent.
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P280-P305+P351+P338-P310
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Hazard InformationBack Directory
[Synthesis]

Indole-6-carboxaldehyde

1196-70-9

Iodoethane

75-03-6

1-ethyl-1H-indole-6-carbaldehyde

854778-47-5

GENERAL METHOD: Cesium carbonate (829 mg, 6 mmol) was added to a solution of indole-6-carboxaldehyde (435 mg, 3 mmol) in acetonitrile (30 mL) and the mixture was heated to reflux for 2 hours. Subsequently, ethyl iodide (3.3 mmol) was added to the reaction system and heating and refluxing was continued for 1 hour. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure, water was added to the residue and extracted three times with ethyl acetate. The organic layers were combined and dried with anhydrous sodium sulfate and subsequently concentrated under vacuum. Finally, the resulting residue was purified by fast column chromatography to afford the target product 1-ethyl-1H-indole-6-carbaldehyde.

[References]

[1] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 7, p. 2060 - 2079
[2] Patent: WO2014/142363, 2014, A1. Location in patent: Paragraph 0405
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