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Indole-5-carboxaldehyde

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Indole-5-carboxaldehyde Basic information

Product Name:
Indole-5-carboxaldehyde
Synonyms:
  • 1H-indol-5-carbaldehyde
  • 1H-INDOLE-5-CARBALDEHYDE
  • 1H-INDOLE-5-CARBOXALDEHYDE
  • 5-INDOLE ALDEHYDE
  • 5-FORMYLINDOLE
  • INDOLE-5-CARBALDEHYDE
  • INDOLE-5-ALDEHYDE
  • INDOLE-5-CARBOXALDEHYDE
CAS:
1196-69-6
MF:
C9H7NO
MW:
145.16
EINECS:
627-955-1
Product Categories:
  • Simple Indoles
  • Building Blocks
  • Indole
  • Building Blocks
  • Indole Derivatives
  • Heterocyclic Building Blocks
  • ALDEHYDE
  • Aldehydes
  • blocks
  • IndolesOxindoles
  • Indoles and derivatives
  • Indoles
  • Heterocycle-Indole series
Mol File:
1196-69-6.mol
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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
pka
16.14±0.30(Predicted)
color 
Orange or tan
Water Solubility 
Insoluble in water.
Sensitive 
Air Sensitive
CAS DataBase Reference
1196-69-6(CAS DataBase Reference)
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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

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Indole-5-carboxaldehyde Usage And Synthesis

Chemical Properties

Red Crystalline Powder

Uses

Reactant 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.

Uses

Indole-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.

Indole-5-carboxaldehyde Preparation Products And Raw materials

Raw materials

Indole-5-carboxaldehydeSupplier

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