All Photos(2)
About This Item
Linear Formula:
CH3(CH2)7I
CAS Number:
Molecular Weight:
240.13
Beilstein/REAXYS Number:
1697479
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
form
liquid
contains
copper as stabilizer
refractive index
n20/D 1.4878 (lit.)
bp
225-226 °C (lit.)
mp
−46-−45 °C (lit.)
density
1.33 g/mL at 25 °C (lit.)
functional group
alkyl halide
iodo
SMILES string
CCCCCCCCI
InChI
1S/C8H17I/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3
InChI key
UWLHSHAHTBJTBA-UHFFFAOYSA-N
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General description
1-Iodooctane undergoes catalytic reduction by nickel (I) salen electrogenerated at a glassy carbon cathode in dimethylformamide. Radical mechanism of formation of monolayer on silicon ground in the presence of 1-iodooctane has been studied by X-ray photoelectron spectroscopy.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Catalytic reduction of 1-iodooctane by nickel (I) salen electrogenerated at carbon cathodes in dimethylformamide: Effects of added proton donors and a mechanism involving both metal-and ligand-centered one-electron reduction of nickel (II) salen.
Raess PW, et al.
Journal of Electroanalytical Chemistry, 603(1), 124-134 (2007)
Evidence for a radical mechanism in monolayer formation on silicon ground (or scribed) in the presence of alkyl halides.
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