3-METHYLOXINDOLE
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
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
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of the class of oxindoles that is oxindole (1,3-dihydro-2H-indol-2-one) in which one of the hydrogens at position 3 has been replaced by a methyl group.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.
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3-METHYLOXINDOLE(1504-06-9)Related Product Information
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- 3,3-BIS(P-HYDROXYPHENYL)OXINDOLE
- GELSEMINE
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- ETHYL 3-HYDROXY-4,6-DIMETHOXY-2-OXOINDOLINE-3-CARBOXYLATE
- 3-PHENYL-OXINDOLE
- 3-hydroxy-3-acetonyl-2-oxindole
- 1,3-Dihydro-3,3-dimethyl-2H-indol-2-one
- 1H-Indole-3-acetonitrile, 2,3-dihydro-2-oxo-
- 3-HYDROXY-3-PHENYLOXINDOLE
- 3-(2-AMINO-ETHYL)-1,3-DIHYDRO-INDOL-2-ONE
- 3-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-1,3-DIHYDRO-2H-INDOL-2-ONE
- 3-METHOXY-1-(4-METHOXYPHENYL)-5-((4-METHYLPHENYL)CARBONYL)SPIRO[AZETIDINE-4,3'-INDOLINE]-2,6-DIONE
- BUTTPARK 58\40-88