46086
7-Ethylindole
≥98.0% (GC)
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About This Item
Empirical Formula (Hill Notation):
C10H11N
CAS Number:
Molecular Weight:
145.20
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
1238356
MDL number:
Assay:
≥98.0% (GC)
SMILES string
CCc1cccc2cc[nH]c12
InChI
1S/C10H11N/c1-2-8-4-3-5-9-6-7-11-10(8)9/h3-7,11H,2H2,1H3
InChI key
PIIZLMYXLGYWTN-UHFFFAOYSA-N
assay
≥98.0% (GC)
impurities
≤0.5% water
refractive index
n20/D 1.603
density
1.058 g/mL at 20 °C (lit.)
storage temp.
2-8°C
Application
- Reactant for preparation of (indo-3-yl) heterocyclic derivatives as agonists of the CB1 receptor
- Reactant for preparation of fluorescent 5H-benzo[b]carbazol-6-yl ketones
- Reactant for preparation of benzoylpiperazinyl-indolyl ethane dione derivatives as HIV-1 inhibitors
- Reactant for preparation of bis(indolyl)alkanehydroxamic acids as histone deacetylase inhibitors
- Reactant for parallel synthesis of indolylquinones as insulin-like compounds
- Reactant for preparation of bis(1H-indol-2-yl)methanones as inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase
Disclaimer
may discolor to deep yellow on storage
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves
Regulatory Information
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D W Old et al.
Organic letters, 2(10), 1403-1406 (2000-05-18)
[equation--see text] The N-arylation of indoles, including a variety of substituted ones, has been carried out using bulky, electron-rich phosphines as the supporting ligand in combination with Pd(2)(dba)(3). Using this catalyst system, the efficient coupling of indole and a variety
Gabriela P S Maciel et al.
Journal of separation science, 38(23), 4071-4077 (2015-10-09)
Although several methods for the analysis of nitrogen compounds in diesel fuel have been described in the literature, the demand for rapid, sensitive, and robust analyses has increased in recent years. In this study, a comprehensive two-dimensional gas chromatographic method
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