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238414

Sigma-Aldrich

1,3-Diiodopropane

99%, contains copper as stabilizer

Synonym(s):

Trimethylene diiodide

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About This Item

Linear Formula:
I(CH2)3I
CAS Number:
627-31-6
Molecular Weight:
295.89
Beilstein/REAXYS Number:
1731117
EC Number:
210-993-4
MDL number:
MFCD00001097
UNSPSC Code:
12352100
PubChem Substance ID:
24854302
NACRES:
NA.22

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.)

storage temp.

2-8°C

SMILES string

ICCCI

InChI

1S/C3H6I2/c4-2-1-3-5/h1-3H2

InChI key

AAAXMNYUNVCMCJ-UHFFFAOYSA-N

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General description

The adsorption of 1,3-diiodopropane on a molybdenum-aluminum alloy thin film formed on dehydroxylated alumina has been studied.

Application

1,3-Diiodopropane has been used in the preparation of synthetically challenging bridged 1,2,4,5-tetraoxanes.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

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

Certificates of Analysis (COA)

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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
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
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

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