Methyl indolyl-3-glyoxylate
Methyl indolyl-3-glyoxylate Basic information
- Product Name:
- Methyl indolyl-3-glyoxylate
- Synonyms:
-
- α-Oxo-1H-indole-3-acetic Acid Methyl Ester
- 1H-Indole-3-acetic acid, α-oxo-, Methyl ester
- Methyl 2-(indol-3-yl)-2-oxoacetate
- Methyl Indol-3-Glyoxylate
- Methyl 3-indoleglyoxylate 98%
- (1H-Indol-3-yl)-oxo-acetic acid methyl ester
- 2-(1H-indol-3-yl)-2-keto-acetic acid methyl ester
- 2-(1H-indol-3-yl)-2-oxoacetic acid methyl ester
- CAS:
- 18372-22-0
- MF:
- C11H9NO3
- MW:
- 203.19
- Product Categories:
-
- Indole Derivatives
- Indole
- Building Blocks
- Heterocyclic Building Blocks
- Indoles
- Mol File:
- 18372-22-0.mol
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Methyl indolyl-3-glyoxylate Chemical Properties
- Melting point:
- 227-230 °C (lit.)
- Boiling point:
- 383.2±15.0 °C(Predicted)
- Density
- 1.324±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Acetone, Methanol
- pka
- 14.54±0.30(Predicted)
- form
- Solid
- color
- Pale Yellow
- Stability:
- Temperature Sensitive
- CAS DataBase Reference
- 18372-22-0(CAS DataBase Reference)
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MSDS
- Language:English Provider:SigmaAldrich
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Methyl indolyl-3-glyoxylate Usage And Synthesis
Chemical Properties
Pale Yellow Fine Powder
Uses
Reactant for preparation of sotrastaurin analogs as protein kinase inhibitors 1 Reactant for synthesis of GSK-3 inhibitors 2 Reactant for Diels-Alder cycloaddition 3 Reactant for preparation of a Janus kinase 3 inhibitor 4 Reactant for synthesis of cephalandole alkaloids 5 Reactant for stereoselective preparation of COX-2 inhibitor as anticancer agent 6 Reactant for synthesis of cycloalkene indole carbazole alkaloids via ring-closing metathesis.
Uses
Methyl Indolyl-3-glyoxylate (cas# 18372-22-0) is a compound useful in organic synthesis.
Methyl indolyl-3-glyoxylateSupplier
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Methyl indolyl-3-glyoxylate(18372-22-0)Related Product Information
- Methyl salicylate
- Indole
- Kresoxim-methyl
- Indometacin
- METSULFURON METHYL
- Methyl acetate
- Methyl benzoate
- Methyl acrylate
- Ethyl glyoxalate
- Methylparaben
- Methyl formate
- Methyl indole-3-carboxylate
- Methyl 2-oxoacetate
- Thiophanate-methyl
- Glyoxylic acid
- 3,3'-Diindolylmethane
- Indole-3-acetic acid
- Indole-3-carboxaldehyde