Substance
ID:331084
Names and Identifiers
IUPAC name
methyl 2-(1H-indol-3-yl)-2-oxoacetate
IUPAC Traditional name
methyl 2-(1H-indol-3-yl)-2-oxoacetate
Synonyms
吲哚-3-乙醛酸甲酯Methyl 2-(indol-3-yl)-2-oxoacetateMethyl 3-indoleglyoxylate
Properties
Safety Information
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
European Hazard Symbols
Irritant (Xi)GHS Hazard statements
H315-H319-H335
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Signal Word
Warning
MSDS Link
GHS Precautionary statements
P261-P305+P351+P338
Safety Statements
26-36
German water hazard class
3
Risk Statements
36/37/38
Product Information
Purity
98%
Empirical Formula (Hill Notation)
C11H9NO3
Physical Property
Melting Point
227-230 °C(lit.)
Molecule Details
Packaging
5 g in glass bottle
Application
• Reactant for preparation of sotrastaurin analogs as protein kinase inhibitors1
• Reactant for synthesis of GSK-3 inhibitors2
• Reactant for Diels-Alder cycloaddition3
• Reactant for preparation of a Janus kinase 3 inhibitor4
• Reactant for synthesis of cephalandole alkaloids5
• Reactant for stereoselective preparation of COX-2 inhibitor as anticancer agent6
• Reactant for synthesis of cycloalkene indole carbazole alkaloids via ring-closing metathesis7
5 g in glass bottle
Application
• Reactant for preparation of sotrastaurin analogs as protein kinase inhibitors1
• Reactant for synthesis of GSK-3 inhibitors2
• Reactant for Diels-Alder cycloaddition3
• Reactant for preparation of a Janus kinase 3 inhibitor4
• Reactant for synthesis of cephalandole alkaloids5
• Reactant for stereoselective preparation of COX-2 inhibitor as anticancer agent6
• Reactant for synthesis of cycloalkene indole carbazole alkaloids via ring-closing metathesis7
Molecular Spectra
No Data Available
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References
No Data Available
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