Basic information Safety Supplier Related

Methyl indolyl-3-glyoxylate

Basic information Safety Supplier Related

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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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2933.99.8290
HazardClass 
IRRITANT

MSDS

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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.

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