| Identification | Back Directory | [Name]
3-METHYLOXINDOLE 96 | [CAS]
1504-06-9 | [Synonyms]
3-Methyloxyindole
3-Methyl-2-oxindole
3-METHYLOXINDOLE 96%
3-METHYLOXINDOLE 96
3-Methyl-2-indolinone
3-methylindolin-2-one
3-Methyl-2-oxindole 96%
3-METHYLOXINDOLE 96 USP/EP/BP
3-Methyl-1,3-dihydro-indol-2-one
1,3-Dihydro-3-Methyl-2H-indol-2-one
3-methyl-2,3-dihydro-1H-indol-2-one
3-Methyl-2-oxindole,3-Methyloxindole
3-Methyloxyindole in stock Factory
2H-Indol-2-one, 1,3-dihydro-3-Methyl-
(R,S)-3-Methyl-1,3-dihydro-indol-2-one | [EINECS(EC#)]
1533716-785-6 | [Molecular Formula]
C9H9NO | [MDL Number]
MFCD04037370 | [MOL File]
1504-06-9.mol | [Molecular Weight]
147.174 |
| Chemical Properties | Back Directory | [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 |
| Hazard Information | Back Directory | [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]
3-Methylindole metabolite. | [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of the class of oxindoles that is oxindole (1,3-dihydro-2H-indol-2-one) in which one of the hydrogens at position 3 has been replaced by a methyl group.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. | [Synthesis]
3-Methylhydroxyindole can be prepared from α-chloropropionyl chloride and aniline in two steps. | [storage]
Store at -20°C |
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CAREBIO PHARMA Gold
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