Basic information Safety Supplier Related

N-ACETYLINDOLE-3-CARBOXALDEHYDE

Basic information Safety Supplier Related

N-ACETYLINDOLE-3-CARBOXALDEHYDE Basic information

Product Name:
N-ACETYLINDOLE-3-CARBOXALDEHYDE
Synonyms:
  • N-ACETYL-3-FORMYLINDOLE
  • N-ACETYLINDOLE-3-ALDEHYDE
  • N-ACETYLINDOLE-3-CARBOXALDEHYDE
  • 1-ACETYLINDOLE-3-CARBALDEHYDE
  • 1-ACETYLINDOLE-3-CARBOXALDEHYDE
  • 1-ACETYL-1H-INDOLE-3-CARBALDEHYDE
  • 1-ACETYL-3-INDOLECARBOXALDEHYDE
  • 1-Acetindole-3-carboxaldehyde
CAS:
22948-94-3
MF:
C11H9NO2
MW:
187.19
EINECS:
245-347-0
Product Categories:
  • Indoles and derivatives
  • IndoleDerivative
  • Aldehydes
  • Pyrroles & Indoles
  • Indole
  • Pyrroles & Indoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • Indoles
Mol File:
22948-94-3.mol
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N-ACETYLINDOLE-3-CARBOXALDEHYDE Chemical Properties

Melting point:
165 °C(lit.)
Boiling point:
336.0±15.0 °C(Predicted)
Density 
1.19±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
Sensitive 
Air Sensitive
CAS DataBase Reference
22948-94-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29339990

MSDS

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N-ACETYLINDOLE-3-CARBOXALDEHYDE Usage And Synthesis

Chemical Properties

White to yellow crystalline powder

Uses

Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture
Reactant for preparation of homoallylic amines as antimicrobial agents
Reactant for preparation of pyrrole-based hydrazones as potential tuberculostatics
Reactant for synthesis of neoechinulin A and derivatives
Reactant for synthesis of substituted (Z)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-one and (Z)-(±)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-ol derivatives as potent thermal sensitizing agents
Reactant for preparation of RNA-specific live cell imaging probes E36, E144 and F22

Definition

ChEBI: 1-acetylindole-3-carboxaldehyde is an N-acylindole that is N-acetylindole carrying an additional formyl substituent at position 3. It has a role as a plant metabolite. It is a N-acylindole and an arenecarbaldehyde.

General Description

1-Acetyl-3-indolecarboxaldehyde participates in the preparation and characterization of three RNA-specific fluorescent probes (E36, E144 and F22), useful in live cell imaging.

N-ACETYLINDOLE-3-CARBOXALDEHYDESupplier

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