ChemicalBook Product Catalog Organic Chemistry Aldehydes Indole-5-carboxaldehyde

Indole-5-carboxaldehyde

Indole-5-carboxaldehyde Basic information
Product Name:Indole-5-carboxaldehyde
Synonyms:1H-indol-5-carbaldehyde;1H-INDOLE-5-CARBOXALDEHYDE;5-INDOLE ALDEHYDE;5-FORMYLINDOLE;INDOLE-5-CARBALDEHYDE;INDOLE-5-ALDEHYDE;INDOLE-5-CARBOXALDEHYDE;5-Formyl-1H-indole
CAS:1196-69-6
MF:C9H7NO
MW:145.16
EINECS:627-955-1
Product Categories:Simple Indoles;Building Blocks;Heterocyclic Building Blocks;Building Blocks;Indole Derivatives;Indole;Indoles;Indoles and derivatives;ALDEHYDE;Aldehydes;blocks;IndolesOxindoles;Heterocycle-Indole series
Mol File:1196-69-6.mol
Indole-5-carboxaldehyde Structure
Indole-5-carboxaldehyde Chemical Properties
Melting point 100-103 °C(lit.)
Boiling point 339.1±15.0 °C(Predicted)
density 1.278±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO, Methanol
form Powder
pka16.14±0.30(Predicted)
color Orange or tan
Water Solubility Insoluble in water.
Sensitive Air Sensitive
CAS DataBase Reference1196-69-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
WGK Germany 3
Hazard Note Irritant/Keep Cold
HazardClass IRRITANT
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
Indole-5-carboxaldehyde Usage And Synthesis
Chemical PropertiesRed Crystalline Powder
UsesReactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents 1 Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors 2 Reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes 3 Reactant in synthesis of para-para stilbenophanes by McMurry coupling 4 Reactant in stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes 5 Reactant in structure-based drug design of aurora kinase A inhibitors.
UsesIndole-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.
2-TERT-BUTYL-1H-INDOLE-3-CARBOXALDEHYDE 1,4-DIMETHYL-3-FORMYLCARBAZOLE 1,2-DIMETHYL-1H-INDOLE-3-CARBOXALDEHYDE 5-carboxamidotryptamine maleate salt 3-FORMYL-1H-INDOLE-5-CARBOXYLIC ACID METHYL ESTER GO 6976 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBOXALDEHYDE 9-BENZYL-3-FORMYLCARBAZOLE 1-BENZYL-2,3-DIMETHYL-1H-INDOLE-5-CARBOXYLIC ACID 1-(4-METHYLBENZENESULFONYL)INDOLE-3-CARBOXALDEHYDE,1-[(4-METHYLPHENYL)SULFONYL]-1H-INDOLE-3-CARBOXALDEHYDE ETHYL 1-OXO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-6-CARBOXYLATE Amindocate VAT BLACK 27 5-CARBOXAMIDOTRYPTAMINE, [1,2-3H]- 5-AMINO-1H-INDOLE-3-CARBOXALDEHYDE HYDROCHLORIDE N,N-DIPROPYL-5-CARBOXAMIDOTRYPTAMINE MALEATE 2-(2-NAPHTHYL)INDOLE-3-CARBOXALDEHYDE STAUROSPORINE
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