129445
Indole-3-carboxaldehyde
97%
Synonym(s):
β-Indolylaldehyde, 3-Formylindole, 3-Indolylformaldehyde, Indole-3-carbaldehyde, NSC 10118
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About This Item
Empirical Formula (Hill Notation):
C9H7NO
CAS Number:
Molecular Weight:
145.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-665-8
Beilstein/REAXYS Number:
114117
MDL number:
Product Name
Indole-3-carboxaldehyde, 97%
InChI key
OLNJUISKUQQNIM-UHFFFAOYSA-N
InChI
1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H
SMILES string
O=Cc1c[nH]c2ccccc12
assay
97%
form
solid
mp
193-198 °C (lit.)
functional group
aldehyde
Quality Level
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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.
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.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Synthetic Communications, 23, 55-55 (1993)
Qiu-Yun Chen et al.
Colloids and surfaces. B, Biointerfaces, 114, 158-163 (2013-11-05)
Multifunctional silica nano-vehicles (SiO2@indol-IL) and magnetic nanoparticles (Fe3O4@indol-IL) were constructed through the Schiff bases condensation of indole-3-carboxaldehyde and 4-acetyl-N-allyl pyridinium chloride (ILs) with the amine groups of silica and magnetic nanoparticles. SiO2@indol-IL can inhibit the proliferation of HepG-2 cells in
Mariana Budovská et al.
Bioorganic & medicinal chemistry, 21(21), 6623-6633 (2013-09-10)
An effective synthesis of analogs of the indole phytoalexin cyclobrassinin with NR1R2 group instead of SCH3 was developed starting from indole-3-carboxaldehyde. The target compounds were prepared by spirocyclization of 1-Boc-thioureas with the formation of isolable spiroindoline intermediates, followed by the
Indian J. Chem. B, 33, 4-4 (1994)
Heterocycles, 38, 1479-1479 (1994)
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