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Key Documents

B5131

Sigma-Aldrich

6-Benzyloxyindole

crystalline

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About This Item

Empirical Formula (Hill Notation):
C15H13NO
CAS Number:
Molecular Weight:
223.27
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Pricing and availability is not currently available.

form

crystalline

color

yellow to brown

storage temp.

2-8°C

SMILES string

C(Oc1ccc2cc[nH]c2c1)c3ccccc3

InChI

1S/C15H13NO/c1-2-4-12(5-3-1)11-17-14-7-6-13-8-9-16-15(13)10-14/h1-10,16H,11H2

InChI key

FPMICYBCFBLGOZ-UHFFFAOYSA-N

Application

  • 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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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    Nenad Manevski et al.
    PloS one, 8(1), e54767-e54767 (2013-02-02)
    Human UDP-glucuronosyltransferases (UGTs) are important enzymes in metabolic elimination of endo- and xenobiotics. It was recently shown that addition of fatty acid free bovine serum albumin (BSA) significantly enhances in vitro activities of UGTs, a limiting factor in in vitro-in

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