- 3-METHYLOXINDOLE 96
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- $0.00 / 25KG
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2023-09-01
- CAS:1504-06-9
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 50000KG/month
- 3-METHYLOXINDOLE 96
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- $9.85 / 1KG
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2021-08-28
- CAS:1504-06-9
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 m
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| | 3-METHYLOXINDOLE 96 Basic information |
| | 3-METHYLOXINDOLE 96 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 |
| WGK Germany | 3 | | HS Code | 2933790090 |
| | 3-METHYLOXINDOLE 96 Usage And Synthesis |
| 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. | | 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 | | 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of the class of oxindoles that is oxindole (1,3-dihydro-2H-indol-2-one) in which one of the hydrogens at position 3 has been replaced by a methyl group.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-METHYLOXINDOLE 96 Preparation Products And Raw materials |
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