Indole-5-carboxylic acid
Indole-5-carboxylic acid
  • CAS No.:1670-81-1
Other grades of this product :
Indole-5-carboxylic acid Basic information
Product Name:Indole-5-carboxylic acid
Synonyms:TIMTEC-BB SBB003951;RARECHEM AL BO 0206;1H-INDOLE-5-CARBOXYLIC ACID;5-CARBOXYINDOLE;5-INDOLECARBOXYLIC ACID;Indolecarboxylicacid,5-;INDOLE-5-CARBOXYLIC ACID;Indole-5-carboxylic acid ,98%
CAS:1670-81-1
MF:C9H7NO2
MW:161.16
EINECS:216-799-6
Product Categories:Heterocycle-Indole series;Simple Indoles;blocks;Carboxes;Building Blocks;Heterocyclic Building Blocks;IndolesOxindoles;Indole/indoline/oxindole;Indole and Indoline;Indoles and derivatives;Indole;Indoles
Mol File:1670-81-1.mol
Indole-5-carboxylic acid Chemical Properties
Melting point 211-213 °C (lit.)
Boiling point 287.44°C (rough estimate)
density 1.2480 (rough estimate)
refractive index 1.5050 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in ethanol (50 mg/ml), dimethyl sulfoxide and methanol.
form Powder
pka4.40±0.30(Predicted)
color Light beige to yellow
BRN 124391
InChIKeyIENZCGNHSIMFJE-UHFFFAOYSA-N
CAS DataBase Reference1670-81-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 36/37/38-21/22
Safety Statements 22-24/25-36/37/39-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29339990
MSDS Information
ProviderLanguage
Indole-5-carboxylic acid English
SigmaAldrich English
ACROS English
ALFA English
Indole-5-carboxylic acid Usage And Synthesis
Chemical Propertieslight beige to yellow powder
UsesReactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, as potential anticancer immunomodulators 1 Reactant for preparation of indolyl-quinolines via metal- and solvent-free autoxidative coupling reaction 2 Reactant for preparation of anthranilic acids using bromamine-B oxidant and palladium chloride catalyst 3 Reactant for synthesis of indirubin derivatives 4 Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway 5 Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity.
UsesIndole-5-carboxylic acid is the suitable reagent used to study the intermolecular excited state proton transfer in indole-2-carboxylic acid and indole-5-carboxylic acid in various solvents in acidic, basic, and neutral media by steady state and time resolved fluorescence spectroscopy. It may be used in the electrochemical synthesis of poly(indole-5-carboxylic acid) (PICA) films. Also used as reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, as potential anticancer immunomodulators, synthesis of indirubin derivatives and amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway.
UsesIndole-5-carboxylic acid is the suitable reagent used to study the intramolecular excited state proton transfer in indole-2-carboxylic acid and indole-5-carboxylic acid in various solvents in acidic, basic, and neutral media by steady state and time resolved fluorescence spectroscopy. It may be used in the electrochemical synthesis of poly(indole-5-carboxylic acid) (PICA) films.
General DescriptionIndole-5-carboxylic acid is an indole derivative. On electropolymerization, it affords electroactive polymer film of poly(indole-5-carboxylic-acid). Different concentrations of indole-5-carboxylic acid in sulfuric acid solution has been investigated for the preventive action against mild steel corrosion. On electropolymerization it affords a trimeric product. Characterization studies of the trimeric product by 1H NMR and various one- and two-dimensional NMR techniques have been reported.
Indole-5-carboxylic acid Preparation Products And Raw materials
Preparation Products1-METHYL-1H-INDOLE-5-CARBOXYLIC ACID-->INDOLE-5-METHANOL-->2,3-DIHYDRO-1H-INDOLE-5-CARBOXYLIC ACID-->Indole-5-carboxaldehyde-->5-Acetylindole

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