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Indole-5-carboxaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: B25517.03
1 g, Each
Thermo Scientific Chemicals
Indole-5-carboxaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: B25517.03
1 g, Each
Quantity
Catalog number: B25517.03
also known as B25517-03
Price (USD)
Price: 45.70
Online price: 39.65
Your price:
Quantity
-
Chemical Identifiers
CAS
1196-69-6
IUPAC Name
1H-indole-5-carbaldehyde
Molecular Formula
C9H7NO
InChI Key
ADZUEEUKBYCSEY-UHFFFAOYSA-N
SMILES
O=CC1=CC=C2NC=CC2=C1
Specifications
Specification SheetAppearance (Color)
Pale cream to cream to orange
Form
Powder
Assay (GC)
≥97.5%
Free acid (titration)
≤1%
Description
Indole-5-carboxaldehyde is used as a reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents; and in synthesis of para-para stilbenophanes by McMurry coupling. It is also used as a reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes and in structure-based drug design of aurora kinase A inhibitors.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Indole-5-carboxaldehyde is used as a reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents; and in synthesis of para-para stilbenophanes by McMurry coupling. It is also used as a reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes and in structure-based drug design of aurora kinase A inhibitors.
Solubility
Insoluble in water.
Notes
Air sensitive. Incompatible with oxidizing agents.
Indole-5-carboxaldehyde is used as a reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents; and in synthesis of para-para stilbenophanes by McMurry coupling. It is also used as a reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes and in structure-based drug design of aurora kinase A inhibitors.
Solubility
Insoluble in water.
Notes
Air sensitive. Incompatible with oxidizing agents.
RUO – Research Use Only
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