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375772 Aldrich

1-Acetyl-3-indolecarboxaldehyde

98%

Synonym: N-Acetylindol-3-carboxaldehyde, NSC 61289

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Properties

Related Categories Aldehydes, Building Blocks, C10-C12, C11, Carbonyl Compounds,
InChI Key   LCJLFGSKHBDOAY-UHFFFAOYSA-N
assay   98%
mp   165 °C(lit.)

Description

Packaging

5 g in glass bottle

Application

1-Acetyl-3-indolecarboxaldehyde may be used to prepare the thiosemicarbazones, via condensation reaction.

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

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.

Price and Availability

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Protocols & Articles

Articles

Indoles

Sigma-Aldrich is proud to offer a new series of ChemFiles—called Privileged Structures, to our Drug Discovery and Organic Synthesis customers. Each piece will highlight a specific motif, selected app...
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Peer-Reviewed Papers
15

References

Related Products

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