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ChemicalBook--->CAS DataBase List--->22948-94-3

22948-94-3

22948-94-3 Structure

22948-94-3 Structure
IdentificationMore
[Name]

N-ACETYLINDOLE-3-CARBOXALDEHYDE
[CAS]

22948-94-3
[Synonyms]

1-ACETYL-1H-INDOLE-3-CARBALDEHYDE
1-ACETYL-3-INDOLECARBOXALDEHYDE
1-ACETYLINDOLE-3-CARBALDEHYDE
1-ACETYLINDOLE-3-CARBOXALDEHYDE
N-ACETYL-3-FORMYLINDOLE
N-ACETYLINDOLE-3-ALDEHYDE
N-ACETYLINDOLE-3-CARBOXALDEHYDE
1-Acetindole-3-carboxaldehyde
l-acetylindole-3-carboxaldehyde
[EINECS(EC#)]

245-347-0
[Molecular Formula]

C11H9NO2
[MDL Number]

MFCD00039691
[Molecular Weight]

187.19
[MOL File]

22948-94-3.mol
Chemical PropertiesBack Directory
[Appearance]

White to yellow crystalline powder
[Melting point ]

165 °C(lit.)
[Boiling point ]

336.0±15.0 °C(Predicted)
[density ]

1.19±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[Sensitive ]

Air Sensitive
[CAS DataBase Reference]

22948-94-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[HS Code ]

29339900
Hazard InformationBack Directory
[Chemical Properties]

White to yellow crystalline powder
[Uses]

Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture
Reactant for preparation of homoallylic amines as antimicrobial agents
Reactant for preparation of pyrrole-based hydrazones as potential tuberculostatics
Reactant for synthesis of neoechinulin A and derivatives
Reactant for synthesis of substituted (Z)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-one and (Z)-(±)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-ol derivatives as potent thermal sensitizing agents
Reactant for preparation of RNA-specific live cell imaging probes E36, E144 and F22
[Definition]

ChEBI: 1-acetylindole-3-carboxaldehyde is an N-acylindole that is N-acetylindole carrying an additional formyl substituent at position 3. It has a role as a plant metabolite. It is a N-acylindole and an arenecarbaldehyde.
[General Description]

1-Acetyl-3-indolecarboxaldehyde participates in the preparation and characterization of three RNA-specific fluorescent probes (E36, E144 and F22), useful in live cell imaging.
Spectrum DetailBack Directory
[Spectrum Detail]

N-ACETYLINDOLE-3-CARBOXALDEHYDE(22948-94-3)MS
N-ACETYLINDOLE-3-CARBOXALDEHYDE(22948-94-3)1HNMR
N-ACETYLINDOLE-3-CARBOXALDEHYDE(22948-94-3)IR1
N-ACETYLINDOLE-3-CARBOXALDEHYDE(22948-94-3)IR2
N-ACETYLINDOLE-3-CARBOXALDEHYDE(22948-94-3)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

N-Acetylindole-3-carboxaldehyde, 98%(22948-94-3)
[Sigma Aldrich]

22948-94-3(sigmaaldrich)
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