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1-Acetylindole

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1-Acetylindole manufacturers

  • 1-ACETYLINDOLE
  • 1-ACETYLINDOLE pictures
  • $7.00
  • 2020-02-19
  • CAS: 576-15-8
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 100kg
1-Acetylindole Basic information
Product Name:1-Acetylindole
Synonyms:1-acetyl-1h-indol;Acetylindole;1H-Indole, 1-acetyl- (9CI);1H-Indole, 1-acetyl-;N-acetoindole;Methyl 1H-indole-1-yl ketone;1-Acetylindole,98%;1-(1H-indol-1-yl)ethanone
CAS:576-15-8
MF:C10H9NO
MW:159.18
EINECS:209-396-1
Product Categories:ACETYLGROUP;Indoles and derivatives;Indole;Building Blocks;Heterocyclic Building Blocks;Indoles
Mol File:576-15-8.mol
1-Acetylindole Structure
1-Acetylindole Chemical Properties
Melting point 189 °C
Boiling point 123-125 °C/8 mmHg (lit.)
density 1.387 g/mL at 25 °C (lit.)
refractive index n20/D 1.607(lit.)
Fp >230 °F
storage temp. 2-8°C
form liquid
AppearanceColorless to light yellow Liquid
Odorat 0.10%indipropylene glycol. floral
InChI1S/C10H9NO/c1-8(12)11-7-6-9-4-2-3-5-10(9)11/h2-7H,1H3
InChIKeyUUCUQJHYUPXDHN-UHFFFAOYSA-N
SMILESCC(=O)n1ccc2ccccc12
LogP2.239 (est)
CAS DataBase Reference576-15-8(CAS DataBase Reference)
EPA Substance Registry System1H-Indole, 1-acetyl- (576-15-8)
Safety Information
Safety Statements 24/25
WGK Germany 3
TSCA TSCA listed
HS Code 29339990
Storage Class10 - Combustible liquids
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
1-Acetylindole Usage And Synthesis
Chemical Propertiesclear yellow liquid after melting
Uses1-Acetylindole may be used in the stereocontrolled synthesis of (±)-geissoschizine. It may be used in the preparation of (1-acetyl-κO-indolyl-κC2)tetracarbonylmanganese, via a standard cyclomanganation procedure.
DefinitionChEBI: N-Acetylindole is a member of indoles.
Synthesis Reference(s)Tetrahedron Letters, 29, p. 2151, 1988 DOI: 10.1016/S0040-4039(00)86696-4
General DescriptionQuantum chemical calculations of ground state energy, geometrical structure and vibrational wavenumbers of 1-acetylindole has been carried out using density functional (DFT/B3LYP) method. Regioselective acylations of 1-acetylindole (N-acetylindole) under Friedel-Crafts reaction has been reported. Reaction of 1-acetylindole with manganese(III) acetate in the presence of malonic acid, is reported to afford 4-acetyl-3,3a,4,8b-tetrahydro-2H-furo[3,2-b]indol-2-one.
1-Acetylindole Preparation Products And Raw materials
Preparation ProductsN-Acetylindole-3-carboxaldehyde
Tag:1-Acetylindole(576-15-8) Related Product Information
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