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1-Methylindole

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1-Methylindole Basic information

Product Name:
1-Methylindole
Synonyms:
  • 1-METHYLINDOLE (N-)
  • 1-METHYLINDOLE
  • 1-METHYLINDOL
  • 1H-Indole, 1-methyl-
  • L-Methylindole
  • 1-METHYLINDOLE, 97+%
  • N-Methyindole
  • 1-Methylindol, 98+%
CAS:
603-76-9
MF:
C9H9N
MW:
131.17
EINECS:
210-057-5
Product Categories:
  • Heterocycle-Indole series
  • Simple Indoles
  • blocks
  • Indoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • IndolesOxindoles
  • Indole
  • bc0001
Mol File:
603-76-9.mol
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1-Methylindole Chemical Properties

Melting point:
61.2°C (estimate)
Boiling point:
133 °C26 mm Hg(lit.)
Density 
1.051 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.606(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Soluble), DMSO (Slightly)
form 
Liquid, May Develop Some Turbidity or Precipitate
color 
Colorless to white
Water Solubility 
insoluble
Sensitive 
Light Sensitive
BRN 
111026
Stability:
Light sensitive. Combustible. Incompatible with strong oxidizing agents.
InChIKey
BLRHMMGNCXNXJL-UHFFFAOYSA-N
LogP
2.720
CAS DataBase Reference
603-76-9(CAS DataBase Reference)
NIST Chemistry Reference
1H-Indole, 1-methyl-(603-76-9)
EPA Substance Registry System
1H-Indole, 1-methyl- (603-76-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-37/39-26
RIDADR 
UN 3334
WGK Germany 
3
13
TSCA 
Yes
HS Code 
29339990

MSDS

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1-Methylindole Usage And Synthesis

Chemical Properties

deep yellow viscous liquid with a very unpleasant smell

Uses

1-Methylindole is useful for the determination of association constant for the electron-donor-acceptor complexes with 1-(2,4,6-trinitrophenyl) propan-2-one. It acts as a reactant for the preparation of polycyclic derivatives of indoles, bisindole derivatives and pharmaceutically active 2-oxo-1-pyrrolidine analogues. It is also used as a reactant for the preparation of Positron Emission Tomography (PET) imaging agents of protein kinase C (PKC) and glycogen synthase kinase-3 (GSK-3).

Synthesis Reference(s)

Synthetic Communications, 26, p. 1349, 1996 DOI: 10.1080/00397919608003495
Tetrahedron Letters, 27, p. 377, 1986 DOI: 10.1016/S0040-4039(00)84023-X

General Description

1-Methylindole undergoes Au(III)/TPPMS-catalyzed benzylation reaction with benzhydryl and benzylic alcohols.

1-MethylindoleSupplier

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