5-Aminoindole

5-Aminoindole
  • CAS No.:5192-03-0
Other grades of this product :
5-Aminoindole Basic information
Product Name:5-Aminoindole
Synonyms:TIMTEC-BB SBB004219;5-AMINO-1H-INDOLE;5-AMINOINDOLE;5-INDOLYLAMINE;5-INDOLAMINE;AKOS 91148;1H-INDOL-5-AMINE;1H-INDOL-5-YLAMINE
CAS:5192-03-0
MF:C8H8N2
MW:132.16
EINECS:225-977-2
Product Categories:Heterocycle-Indole series;Amines;IndoleDerivative;Indole Derivatives;Simple Indoles;Aromatics;indole derivative;Indoles and derivatives;Indoles
Mol File:5192-03-0.mol
5-Aminoindole Chemical Properties
Melting point 131-133 °C (dec.) (lit.)
Boiling point 190 °C / 6mmHg
density 1.1083 (rough estimate)
refractive index 1.6013 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO, Methanol
pka17.39±0.30(Predicted)
form Crystalline Powder
color Off-white to gray-brown
Water Solubility insoluble
Sensitive Air & Light Sensitive
BRN 112348
InChIKeyZCBIFHNDZBSCEP-UHFFFAOYSA-N
CAS DataBase Reference5192-03-0(CAS DataBase Reference)
NIST Chemistry Reference5-Aminoindole(5192-03-0)
EPA Substance Registry System5-Aminoindole (5192-03-0)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-68
Safety Statements 26-45-36/37
WGK Germany 3
10
Hazard Note Irritant
TSCA Yes
HazardClass AIR SENSITIVE, IRRITANT-HARMFUL, KEEP COLD
HS Code 29339990
MSDS Information
ProviderLanguage
5-Aminoindole English
SigmaAldrich English
ACROS English
ALFA English
5-Aminoindole Usage And Synthesis
Chemical PropertiesGrey Crystals
UsesReactant for preparation of:
  • Smac mimetics that bind to the BIR2 domain of the anti-apoptotic protein XIAP
  • Cytotoxic and antimitotic agents
  • Insulin-like growth factor 1 receptor inhibitors
  • Antitumoral agents
  • Factor Xa inhibitor
  • Potential antivascular agents
  • Gli1-mediated transcription in the Hedgehog pathway
  • Inhibitors of receptor tyrosine kinase with antiangiogenic effects
  • PKCθ inhibitors
  • HIV protease inhibitors
Uses5-Aminoindole functions as a ligand for hydrophobic charge induction chromatography. A reagent for synthetic elaboration.
DefinitionChEBI: An indolamine carrying an amino group at position 5.
5-Aminoindole Preparation Products And Raw materials
Raw materialsEthanol-->Iron-->Polyphosphoric acid-->Quinoline-->Ethyl pyruvate-->Cupric oxide-->4-Nitrophenylhydrazine

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