Basic information Safety Supplier Related

Methyl indole-4-carboxylate

Basic information Safety Supplier Related

Methyl indole-4-carboxylate Basic information

Product Name:
Methyl indole-4-carboxylate
Synonyms:
  • Methyl indole-4-carboxylate ,99%
  • methylindole-4-carboxylate , (4-indole-carboxylic acid methyl ester)
  • METHYL-1H-INDOLE-4-CARBOXYLATE
  • Methyl indole-4-carboxylate ,98%
  • Methyl indole-4-carboxyla...
  • 4-(Methoxycarbonyl)-1H-indole
  • 4-Methoxycarbonylindole
  • RARECHEM AH BS 0113
CAS:
39830-66-5
MF:
C10H9NO2
MW:
175.18
EINECS:
622-802-5
Product Categories:
  • Building Blocks
  • C10
  • Indoles and derivatives
  • pharmacetical
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • blocks
  • Carboxes
  • IndolesOxindoles
  • Indole
  • Indoles
  • Simple Indoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • Acids and Derivatives
  • Heterocycles
Mol File:
39830-66-5.mol
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Methyl indole-4-carboxylate Chemical Properties

Melting point:
68-71 °C(lit.)
Boiling point:
306.47°C (rough estimate)
Density 
1.1999 (rough estimate)
refractive index 
1.5060 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
Crystalline Powder
pka
15.80±0.30(Predicted)
color 
Off-white to green
BRN 
141826
InChIKey
WEAXQUBYRSEBJD-UHFFFAOYSA-N
CAS DataBase Reference
39830-66-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900

MSDS

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Methyl indole-4-carboxylate Usage And Synthesis

Chemical Properties

off-white to green crystalline powder

Uses

• ;Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1• ;Reactant for preparation of cytotoxic agents against multidrug-resistant cancer cells2• ;Reactant for preparation of inhibitor for β-tryptase3• ;Reactant for preparation of histamine H3 antagonists4• ;Reactant for preparation of JNK3 MAP kinase inhibitors5• ;Reactant for preparation of nucleosides6

Uses

  • Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
  • Reactant for preparation of cytotoxic agents against multidrug-resistant cancer cells
  • Reactant for preparation of inhibitor for β-tryptase
  • Reactant for preparation of histamine H3 antagonists
  • Reactant for preparation of JNK3 MAP kinase inhibitors
  • Reactant for preparation of nucleosides

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 26, p. 1405, 1989 DOI: 10.1002/jhet.5570260533
Chemical and Pharmaceutical Bulletin, 29, p. 249, 1981 DOI: 10.1248/cpb.29.249

General Description

The IR and UV spectra of methyl indole-4-carboxylate was studied.

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