380490
(2-Iodoethyl)benzene
97%
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About This Item
Linear Formula:
C6H5CH2CH2I
CAS Number:
Molecular Weight:
232.06
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
(2-Iodoethyl)benzene, 97%
InChI
1S/C8H9I/c9-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2
SMILES string
ICCc1ccccc1
InChI key
KVTHPKXDLVYNCH-UHFFFAOYSA-N
assay
97%
form
liquid
refractive index
n20/D 1.601 (lit.)
bp
122-123 °C/13 mmHg (lit.)
density
1.603 g/mL at 25 °C (lit.)
functional group
iodo
phenyl
Quality Level
Related Categories
Application
(2-Iodoethyl)benzene is suitable for use as starting reagent in the preparation of organic-inorganic hybrid compounds such as, [C6H5CH2NH3]2PbI4, [C6H5CH2CH2SC(NH2 )2]3PbI5 and [C10H7CH2NH3]PbI3. It may be used in the preparation of dioxane-based antiviral agents.
General description
(2-Iodoethyl)benzene is a halogenated hydrocarbon. It is reported to undergo triethyl borane-mediated intermolecular radical addition with 2H-azirine-3-carboxylate.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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Ha Young Kim et al.
Bioorganic & medicinal chemistry letters, 15(13), 3207-3211 (2005-06-02)
Dioxane-based antiviral agents targeted to the hydrophobic binding pocket of Sindbis virus capsid protein were designed by computer graphics molecular modeling and synthesized. Virus production using SIN-IRES-Luc and capsid assembly were monitored to evaluate antiviral activity. A compound with a
Intermolecular alkyl radical addition to methyl 2-(2, 6-dichlorophenyl)-2H-azirine-3-carboxylate.
Lemos A, et al.
Synlett, 10, 1403-1406 (2003)
Preparation and Characterization of [C6H5CH2NH3] 2PbI4,[C6H5CH2CH2SC (NH2) 2] 3PbI5 and [C10H7CH2NH3] PbI3 Organic-Inorganic Hybrid Compounds.
Papavassiliou GC, et al.
Zeitschrift fur Naturforschung, 54b, 1405-1405 (1999)
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