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ChemicalBook--->CAS DataBase List--->15903-94-3

15903-94-3

15903-94-3 Structure

15903-94-3 Structure
IdentificationMore
[Name]

6-Benzyloxyindole
[CAS]

15903-94-3
[Synonyms]

6-BENZYLOXYINDOLE
6-(Benzyloxy)-1H-indole
NSC 92538
6-(Phenylmethoxy)-1H-indole
6-(Benzyloxy)-1H-indole 98%
6-BENZYLOXYINDOLE 97%
6-Benzyloxyindole ,98%
[EINECS(EC#)]

810-565-2
[Molecular Formula]

C15H13NO
[MDL Number]

MFCD00053554
[Molecular Weight]

223.27
[MOL File]

15903-94-3.mol
Chemical PropertiesBack Directory
[Appearance]

Colourless Crystalline Solid
[Melting point ]

116-119°C
[Boiling point ]

411.6±20.0 °C(Predicted)
[density ]

1.196±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Diethyl Ether (Slightly), Ethanol (Slightly), Ethyl Aceta
[form ]

crystalline
[pka]

17.17±0.30(Predicted)
[color ]

yellow to brown
[Usage]

Indole derivative, as antiviral and antitumor agent
[Detection Methods]

HPLC,NMR
[BRN ]

173319
[InChIKey]

FPMICYBCFBLGOZ-UHFFFAOYSA-N
[CAS DataBase Reference]

15903-94-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[Hazard Note ]

Irritant/Keep Cold
[HS Code ]

29339900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->N,N-Dimethylformamide-->Potassium carbonate-->Acetone-->Hydrazinium hydroxide solution-->Benzyl chloride-->N,N-Dimethylformamide dimethyl acetal-->Pyrrolidine-->Palladium chloride-->4-Methyl-3-nitrophenol-->NICKEL BORIDE
[Preparation Products]

2-Acetamido-3-(6-(benzyloxy)-1H-indol-3-yl)propanoic acid
Hazard InformationBack Directory
[Chemical Properties]

Colourless Crystalline Solid
[Uses]

  • Reactant for enantioselective synthesis of quaternary carbon-containing 3-(3-indolyl)isoindolin-1-ones
  • Reactant for Friedel-Crafts alkylation reactions with hydroxyisoindolinones
  • Reactant for direct and regioselective synthesis of β-heteroarylated ketones
  • Reactant for preparation of hepatitis C virus (HCV) inhibitors
  • Reactant for preparation of protein kinase C (PKC) inhibitors
  • Reactant for preparation of indol-3-yl tetramethylcyclopropyl ketones as CB2 cannabinoid receptor ligands
[Uses]

Indole derivative, as antiviral and antitumor agent
Spectrum DetailBack Directory
[Spectrum Detail]

6-Benzyloxyindole(15903-94-3)MS
6-Benzyloxyindole(15903-94-3)1HNMR
6-Benzyloxyindole(15903-94-3)13CNMR
6-Benzyloxyindole(15903-94-3)IR1
6-Benzyloxyindole(15903-94-3)IR2
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

6-Benzyloxyindole, 97%(15903-94-3)
[Sigma Aldrich]

15903-94-3(sigmaaldrich)
[TCI AMERICA]

6-Benzyloxyindole,>98.0%(GC)(N)(15903-94-3)
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