Indole-6-carboxylic acid

Indole-6-carboxylic acid
  • CAS No.:1670-82-2
Other grades of this product :
Indole-6-carboxylic acid Basic information
Product Name:Indole-6-carboxylic acid
Synonyms:6-INDOLECARBOXYLIC ACID;Indole-6-carboxylic acid in stock Factory;6-CARBOXYINDOLE;4-CARBOXAMIDOBENZOIC ACID;1H-INDOLE-6-CARBOXYLIC ACID;LABOTEST-BB LT00441293;INDOLE-6-CARBOXYLIC ACID;RARECHEM AL BE 1265
CAS:1670-82-2
MF:C9H7NO2
MW:161.16
EINECS:605-464-3
Product Categories:Heterocycle-Indole series;Heterocyclic Building Blocks;Simple Indoles;Building Blocks;C7 to C9;Chemical Synthesis;blocks;Carboxes;IndolesOxindoles;Indole;Carboxylic Acids;Pyrroles & Indoles;Building Blocks;Heterocyclic Building Blocks;Indole/indoline/oxindole;Indole and Indoline;Indoles and derivatives;Carboxylic Acids;Pyrroles & Indoles;Organic acids;Indoles
Mol File:1670-82-2.mol
Indole-6-carboxylic acid Chemical Properties
Melting point 249-253 °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
pka4.44±0.30(Predicted)
form Powder
color Yellow-beige to orange-brown
BRN 123991
CAS DataBase Reference1670-82-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 36/37/38-21/22-20/21/22-51-36-22
Safety Statements 22-24/25-37/39-26
WGK Germany 3
Hazard Note Irritant
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
Indole-6-carboxylic acid Usage And Synthesis
Chemical Propertiesyellow-beige to orange-brown powder
Uses• ;Reactant for preparation of D-glutamic acid-based inhibitors of E. coli MurD ligase1• ;Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors2• ;Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway3• ;Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity4• ;Reactant for preparation of pyridinyl carboxylates via esterification with chlorohyd
UsesReactant for preparation of D-glutamic acid-based inhibitors of E. coli MurD ligase ? Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors ? Reactant for preparation of amide conju
Uses
  • Reactant for preparation of D-glutamic acid-based inhibitors of E. coli MurD ligase
  • Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors
  • Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway
  • Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity
  • Reactant for preparation of pyridinyl carboxylates via esterification with chlorohydroxypyridine as SARS-CoV 3CL proinhibitors
  • Reactant for preparation of (indolecarbonyl)-D-phenylglycinamide amides as factor Xa inhibitors
Synthesis Reference(s)Journal of Medicinal Chemistry, 35, p. 2419, 1992 DOI: 10.1021/jm00091a010
Indole-6-carboxylic acid Preparation Products And Raw materials
Raw materialsSodium hydroxide-->Hydrochloric acid-->Methanol-->Tetrahydrofuran-->N,N-Dimethylformamide-->Palladium-->N,N-Dimethylformamide dimethyl acetal-->Pyrrolidine-->4-Methyl-3-nitrobenzoic acid
Preparation ProductsAKOS B006681

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