238414
1,3-二碘丙烷
99%, contains copper as stabilizer
别名:
三亚甲基二碘化物
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关于此项目
线性分子式:
I(CH2)3I
化学文摘社编号:
分子量:
295.89
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-993-4
Beilstein/REAXYS Number:
1731117
MDL number:
产品名称
1,3-二碘丙烷, 99%, contains copper as stabilizer
InChI key
AAAXMNYUNVCMCJ-UHFFFAOYSA-N
InChI
1S/C3H6I2/c4-2-1-3-5/h1-3H2
SMILES string
ICCCI
assay
99%
form
liquid
contains
copper as stabilizer
refractive index
n20/D 1.642 (lit.)
bp
111-113 °C/31 mmHg (lit.)
density
2.576 g/mL at 25 °C (lit.)
functional group
iodo
storage temp.
2-8°C
Quality Level
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Application
1,3-Diiodopropane has been used in the preparation of synthetically challenging bridged 1,2,4,5-tetraoxanes.
General description
The adsorption of 1,3-diiodopropane on a molybdenum-aluminum alloy thin film formed on dehydroxylated alumina has been studied.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Feng Gao et al.
The journal of physical chemistry. B, 110(25), 12555-12571 (2006-06-28)
The adsorption of C3 hydrocarbons propylene, 1-iodopropane, and 1,3-diiodopropane is studied in ultrahigh vacuum on a molybdenum-aluminum alloy formed by molybdenum hexacarbonyl reaction with a planar alumina film grown on a Mo(100) substrate. Carbon-iodine bond scission occurs below approximately 200
Gemma L Ellis et al.
Bioorganic & medicinal chemistry letters, 18(5), 1720-1724 (2008-02-05)
Here we present an efficient route into synthetically challenging bridged 1,2,4,5-tetraoxanes. The key to the success of this route is the use of H(2)O(2) and catalytic I(2) to form the gem-dihydroperoxide followed by a Ag(2)O mediated alkylation using 1,3-diiodopropane. Using
Shyamala Pillai et al.
Journal of fluorescence, 22(4), 1021-1032 (2012-03-28)
A variety of contemporary analytical platforms, utilized in technical and biological applications, take advantage of labeling the objects of interest with fluorescent tracers-compounds that can be easily and sensitively detected. Here we describe the synthesis of new fluorescent quinoline and
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