5-Methoxyindole-3-c...

5-Methoxyindole-3-carboxaldehyde  10601-19-1

5-Methoxyindole-3-carboxaldehyde 10601-19-1

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1 Kilogram

FOB Price: USD 300.0000

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,T/T

Keywords

5-Methoxyindole-3-carboxaldehyde 10601-19-1 5-Methoxyindole-3-carboxaldehyde 10601-19-1 5-Methoxyindole-3-carboxaldehyde 10601-19-1

Quick Details

  • Appearance:Powder
  • Application:Organic Chemicals
  • PackAge:as requested
  • ProductionCapacity:100|Metric Ton|Day
  • Storage:room temperature
  • Transportation:BY SEA

Superiority:

Product Name: 5-Methoxyindole-3-carboxaldehyde
Synonyms: 5-Methoxyindole-3-carboxaldehyde, 3-Formyl-5-methoxyindole;3-Formyl-5-methoxyindole,>99%;5-methoxyindole-3-formaldehyde (5-methoxyindole-3-carboxyaldehyde);5-METHOXY-3-CARBOXALDEHYDEINDOLE;1H-indole-3-carboxaldehyde, 5-methoxy-;5-METHOXYINDOLE-3-CARBOXALDEHYDEINDOCIN INFREE RANTUDIL;5-Methoxyindole-3-Carboxaldehhvde;1H-indole-3-carbaldehyde, 5-methoxy
CAS: 10601-19-1
MF: C10H9NO2
MW: 175.18
EINECS: 234-220-5
Product Categories: blocks;Carboxes;IndolesOxindoles;Heterocycles;Indoles and derivatives;IndoleDerivative;Aldehydes;Pyrroles & Indoles;Indoline & Oxindole;Building Blocks;Indole;Indoles;Simple Indoles;Chiral Compound;Intermediates of Tegaserod;Pyrroles & Indoles;Building Blocks;Heterocyclic Building Blocks;Heterocycle-Indole series
Mol File: 10601-19-1.mol

5-Methoxyindole-3-carboxaldehyde Chemical Properties
Melting point  179-183 °C(lit.)
Boiling point  306.47°C (rough estimate)
density  1.1999 (rough estimate)
refractive index  1.5060 (estimate)
pka 15.21±0.30(Predicted)
form  Crystalline Powder or Needles
color  Yellow to beige
Water Solubility  insoluble
Sensitive  Air Sensitive
BRN  132769
CAS DataBase Reference 10601-19-1(CAS DataBase Reference)
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-26
WGK Germany  3
HazardClass  IRRITANT, AIR SENSITIVE
HS Code  29339900

5-Methoxyindole-3-carboxaldehyde Usage And Synthesis
Chemical Properties yellowish to beige crystalline powder or needles
Uses reactant in synthesis of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators 1 reactant in preparation of inhibitor of the C-terminal domain of RNA polymerase II reactant in preparation of imidazopyridines and imidazobenzothiazoles 2 reactant in preparation of fluorescent neuroactive probes for brain imaging 3 reactant in preparation of antibacterial agents 4 reactant in synthesis of antiandrogens.

Details:

Product Name: 5-Methoxyindole-3-carboxaldehyde
Synonyms: 5-Methoxyindole-3-carboxaldehyde, 3-Formyl-5-methoxyindole;3-Formyl-5-methoxyindole,>99%;5-methoxyindole-3-formaldehyde (5-methoxyindole-3-carboxyaldehyde);5-METHOXY-3-CARBOXALDEHYDEINDOLE;1H-indole-3-carboxaldehyde, 5-methoxy-;5-METHOXYINDOLE-3-CARBOXALDEHYDEINDOCIN INFREE RANTUDIL;5-Methoxyindole-3-Carboxaldehhvde;1H-indole-3-carbaldehyde, 5-methoxy
CAS: 10601-19-1
MF: C10H9NO2
MW: 175.18
EINECS: 234-220-5
Product Categories: blocks;Carboxes;IndolesOxindoles;Heterocycles;Indoles and derivatives;IndoleDerivative;Aldehydes;Pyrroles & Indoles;Indoline & Oxindole;Building Blocks;Indole;Indoles;Simple Indoles;Chiral Compound;Intermediates of Tegaserod;Pyrroles & Indoles;Building Blocks;Heterocyclic Building Blocks;Heterocycle-Indole series
Mol File: 10601-19-1.mol

5-Methoxyindole-3-carboxaldehyde Chemical Properties
Melting point  179-183 °C(lit.)
Boiling point  306.47°C (rough estimate)
density  1.1999 (rough estimate)
refractive index  1.5060 (estimate)
pka 15.21±0.30(Predicted)
form  Crystalline Powder or Needles
color  Yellow to beige
Water Solubility  insoluble
Sensitive  Air Sensitive
BRN  132769
CAS DataBase Reference 10601-19-1(CAS DataBase Reference)
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-26
WGK Germany  3
HazardClass  IRRITANT, AIR SENSITIVE
HS Code  29339900

5-Methoxyindole-3-carboxaldehyde Usage And Synthesis
Chemical Properties yellowish to beige crystalline powder or needles
Uses reactant in synthesis of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators 1 reactant in preparation of inhibitor of the C-terminal domain of RNA polymerase II reactant in preparation of imidazopyridines and imidazobenzothiazoles 2 reactant in preparation of fluorescent neuroactive probes for brain imaging 3 reactant in preparation of antibacterial agents 4 reactant in synthesis of antiandrogens.

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