B5131
6-Benzyloxyindole
crystalline
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About This Item
Empirical Formula (Hill Notation):
C15H13NO
CAS Number:
Molecular Weight:
223.27
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Form:
crystalline
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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| B5131-250MG | 04061832842486 |