Substance
ID:333389
Names and Identifiers
IUPAC Traditional name
N-methylindol-2,3-dione
IUPAC name
1-methyl-2,3-dihydro-1H-indole-2,3-dione
Synonyms
1-MethylisatinNSC 42449N-Methylindoline-2,3-dione1-甲基靛红
Properties
Product Information
Empirical Formula (Hill Notation)
C9H7NO2
Purity
97%
Safety Information
Hazard Class
6.1
Packing Group
3
RTECS
NL7939000
German water hazard class
3
GHS Hazard statements
H301-H315-H318-H335
GHS Signal Word
Danger
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
MSDS Link
European Hazard Symbols
Toxic (T)GHS Precautionary statements
P261-P280-P301+P310-P305+P351+P338
Risk Statements
25-37/38-41
UN Number
2811
Personal Protective Equipment
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
RID/ADR
UN 2811 6.1/PG 3
Safety Statements
26-39-45
Pharmacology Properties
Gene Information
human ... CASP3(836)
Physical Property
Melting Point
130-133 °C(lit.)
Molecule Details
Packaging
1, 10 g in glass bottle
Application
• Reactant for stereoselective preparation of spirobicyclic and bis-spirotricyclic pyrazolidinones1
• Reactant for regioselective preparation of spirocyclic oxindole-butenolides2
• Reactant for synthesis of spiro-oxindoles3
• Reactant for preparation of unsymmetrical oxindoles4
• Reactant for stereoselective preparation of hydroxyloxindoles via Morita-Baylis-Hillman reaction4
• Reactant for preparation of pyridinecarboxylic acid [(oxo)indolylidene)hydrazide derivatives (Schiff base hydrazides) as antibacterial agents5
1, 10 g in glass bottle
Application
• Reactant for stereoselective preparation of spirobicyclic and bis-spirotricyclic pyrazolidinones1
• Reactant for regioselective preparation of spirocyclic oxindole-butenolides2
• Reactant for synthesis of spiro-oxindoles3
• Reactant for preparation of unsymmetrical oxindoles4
• Reactant for stereoselective preparation of hydroxyloxindoles via Morita-Baylis-Hillman reaction4
• Reactant for preparation of pyridinecarboxylic acid [(oxo)indolylidene)hydrazide derivatives (Schiff base hydrazides) as antibacterial agents5
Molecular Spectra
No Data Available
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References
No Data Available
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