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About This Item
Linear Formula:
ICH2CH2I
CAS Number:
Molecular Weight:
281.86
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-859-5
Beilstein/REAXYS Number:
1730870
MDL number:
Assay:
99%
Form:
powder or crystals
Quality Level
assay
99%
form
powder or crystals
mp
80-82 °C (lit.)
density
2.132 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
ICCI
InChI
1S/C2H4I2/c3-1-2-4/h1-2H2
InChI key
GBBZLMLLFVFKJM-UHFFFAOYSA-N
Application
1,2-Diiodoethane can be used:
- To synthesize samarium(II) iodide-water complex (SmI2-H2O complex), a single-electron transfer reagent, to further synthesize 3-hydroxy carboxylic acids.
- To synthesize derivatives of regioselective homopropargyl alcohols by using sonochemical Barbier-type reaction conditions.
- As an iodine source and an effective reagent for the dehydroxy-iodination of alcohols.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of homopropargyl alcohols via sonochemical Barbier-type reaction.
Lee ASY, et al.
Tetrahedron Letters, 45(7), 1551-1553 (2004)
Halogenation through Deoxygenation of Alcohols and Aldehydes.
Chen J, et al.
Organic Letters, 20(10), 3061-3064 (2018)
Michal Szostak et al.
Nature protocols, 7(5), 970-977 (2012-04-28)
The single-step synthesis of 3-hydroxy carboxylic acids from readily available Meldrum's acids involves a selective monoreduction using a SmI(2)-H(2)O complex to give products in high crude purity, and it represents a considerable advancement over other methods for the synthesis of
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D122807-25G | 04061833559048 |
| D122807-100G | 04061833563175 |
