Basic information Safety Supplier Related

3-METHYLOXINDOLE

Basic information Safety Supplier Related

3-METHYLOXINDOLE Basic information

Product Name:
3-METHYLOXINDOLE
Synonyms:
  • 3-Methyloxyindole in stock Factory
  • 3-Methyl-2-oxindole,3-Methyloxindole
  • 1,3-Dihydro-3-Methyl-2H-indol-2-one
  • 3-Methyl-2-indolinone
  • 2H-Indol-2-one, 1,3-dihydro-3-Methyl-
  • 3-Methyl-2-oxindole 96%
  • 3-methylindolin-2-one
  • 3-methyl-2,3-dihydro-1H-indol-2-one
CAS:
1504-06-9
MF:
C9H9NO
MW:
147.17
EINECS:
1533716-785-6
Product Categories:
  • Aromatics, Indole Derivatives, Metabolites & Impurities
  • Aromatics
  • Indole Derivatives
  • Metabolites & Impurities
  • Building Blocks
  • C7 to C9
  • Heterocyclic Compounds
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Indoles
Mol File:
1504-06-9.mol
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3-METHYLOXINDOLE Chemical Properties

Melting point:
117-121 °C(lit.)
Boiling point:
279.3±29.0 °C(Predicted)
Density 
1.123±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethanol (Slightly), Methanol (Slightly)
form 
Solid
pka
14.81±0.40(Predicted)
color 
Light Beige to Beige
Water Solubility 
Insoluble in water.
CAS DataBase Reference
1504-06-9
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Safety Information

WGK Germany 
3
HS Code 
2933790090
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3-METHYLOXINDOLE Usage And Synthesis

Uses

• ;Reactant for enantioselective α-amination reactions1• ;Reactant for aldol reaction with glyoxal derivatives2• ;Reactant for amine thiourea catalyzed conjugate addition to α,β-unsaturated aldehydes3• ;Reactant for O-acetylation reactions4• ;Reactant for preparation of a disubstituted oxoindole by using rhodium-catalyzed cyclopropanation/ring-opening reactions5

Uses

A versatile reactant. As 3-Methylindole metabolite. Reactant for enantioselective α-amination reactions, Reactant for aldol reaction with glyoxal derivatives, Reactant for amine thiourea catalyzed conjugate addition to α,β-unsaturated aldehydes, Reactant for O-acetylation reactions, Reactant for preparation of a disubstituted oxoindole by using rhodium-catalyzed cyclopropanation/ring-opening reactions.

Definition

ChEBI: 3-methyloxindole is a member of the class of oxindoles that is oxindole (1,3-dihydro-2H-indol-2-one) in which one of the hydrogens at position 3 has been replaced by a methyl group. It is a member of oxindoles and a methylindole.

General Description

3-Methyl-2-oxindole (MOI) is a 3-substituted-2-oxindole. It is reported to be formed during the oxidation of indole-3-acetic acid in the presence of FeII under aerobic conditions. MOI undergoes asymmetric anti-Mannich-type reaction with N-tosyl aryl aldimines in the presence of alkaloid cinchona derivatives to form anti-3,3-disubsituted 2-oxindole derivatives. It also undergoes asymmetric hydroxyamination with nitrosoarenes to form N-nitroso aldol products.

3-METHYLOXINDOLESupplier

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