Recommended Products
Quality Level
Assay
98%
mp
227-230 °C (lit.)
SMILES string
COC(=O)C(=O)c1c[nH]c2ccccc12
InChI
1S/C11H9NO3/c1-15-11(14)10(13)8-6-12-9-5-3-2-4-7(8)9/h2-6,12H,1H3
InChI key
VFIJGAWYVXDYLK-UHFFFAOYSA-N
Related Categories
Application
- Reactant for preparation of sotrastaurin analogs as protein kinase inhibitors
- Reactant for synthesis of GSK-3 inhibitors
- Reactant for Diels-Alder cycloaddition
- Reactant for preparation of a Janus kinase 3 inhibitor
- Reactant for synthesis of cephalandole alkaloids
- Reactant for stereoselective preparation of COX-2 inhibitor as anticancer agent
- Reactant for synthesis of cycloalkene indole carbazole alkaloids via ring-closing metathesis
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 19(1), 123-127 (2003-02-01)
The chemiluminescence (CL) intensities of various indole derivatives substituted with a glyoxylyl group at the 3-position and a hydroxyl group at the 5-position of the indole ring were compared upon the addition of H2O2 in alkaline media. The CL intensities
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