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Indole-3-carboxaldehyde

ALDRICH/129445 - 97%

Synonym: β-Indolylaldehyde; 3-Formylindole; 3-Indolylformaldehyde; Indole-3-carbaldehyde; NSC 10118

CAS Number: 487-89-8
Empirical Formula (Hill Notation): C9H7NO
Molecular Weight: 145.16
EC Number: 207-665-8
MDL Number: MFCD00005622
Linear Formula: C9H7NO
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-129445-5G 5 g
$37.10
1/EA
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45-129445-25G 25 g
$86.90
1/EA
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assay 97%
form solid
InChI 1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H
InChI key OLNJUISKUQQNIM-UHFFFAOYSA-N
mp 193-198 °C (lit.)
Quality Level 200 
SMILES string O=Cc1c[nH]c2ccccc12
Application: Indole-3-carboxaldehyde was used to prepare analogs of the indole phytoalexin cyclobrassinin with NR1R2 group. It was also used as the starting material for the synthesis of higher order indoles including isoindolo[2,1-a]indoles, aplysinopsins, and 4-substituted-tetrahydrobenz[cd]indoles.
Application: Reactant for preparation of:
• Analgesic agents
• Hypoglycemic agents
• Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
• Antibacterial and antifungal agents
• Antiamoebic and cytotoxic agents
• Inhibitors of the Dengue virus protease with antiviral activity in cell-culture
• Curcumin analogues as possible anti-proliferative & anti-inflammatory agents
• Inhibitors of Bcl-2 family proteins
• Inhibitors of the C-terminal domain of RNA Polymerase II as antitumor agents
• Inhibitors of TNF-α and IL-6 with anti-tubercular activity
General description: Indole-3-carboxaldehyde can undergo Schiff bases condensation to form multifunctional silica nano-vehicles and magnetic nanoparticles.
Packaging: 25 g in poly bottle
Packaging: 5 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity 97%
mp 193-198 °C (lit.)
UNSPSC 12352100

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