ChemicalBook > Product Catalog > Organic Chemistry > Hydrocarbons and derivatives > Hydrocarbon halides > 1,2-DIIODOETHANE
1,2-DIIODOETHANE
1,2-DIIODOETHANE Basic information
- Product Name:
- 1,2-DIIODOETHANE
- Synonyms:
-
- 1,2-DIIODOETHANE
- ETHYLENE DIIODIDE
- ETHYLENE IODIDE
- 1,2-Diiodoethane,98%
- Ethylenjodid
- Glycoldiiodide
- JACS-624-73-7
- 1,2-Diiodoethane ,98.5%
- CAS:
- 624-73-7
- MF:
- C2H4I2
- MW:
- 281.86
- EINECS:
- 210-859-5
- Product Categories:
-
- Alkyl
- Building Blocks
- Chemical Synthesis
- Halogenated Hydrocarbons
- Organic Building Blocks
- Mol File:
- 624-73-7.mol
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1,2-DIIODOETHANE Chemical Properties
- Melting point:
- 80-82 °C (lit.)
- Boiling point:
- 200.05°C
- Density
- 2.132 g/mL at 25 °C (lit.)
- refractive index
- 1.8710
- storage temp.
- 2-8°C
- form
- Crystals or Crystalline Powder
- Specific Gravity
- 2.132
- color
- Light brown to brown
- Water Solubility
- Soluble in methanol. Insoluble in water.
- Sensitive
- Air & Light Sensitive
- BRN
- 1730870
- Dielectric constant
- 3.4(Ambient)
- Stability:
- Stable, but may discolour on exposure to light. Incompatible with strong bases, strong oxidizing agents.
- CAS DataBase Reference
- 624-73-7(CAS DataBase Reference)
- EPA Substance Registry System
- Ethane, 1,2-diiodo- (624-73-7)
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Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- RIDADR
- 2811
- WGK Germany
- 3
- F
- 8-9-23
- TSCA
- Yes
- HazardClass
- 6.1(b)
- PackingGroup
- III
- HS Code
- 29033990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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1,2-DIIODOETHANE Usage And Synthesis
Chemical Properties
dark brown crystals
Uses
1,2-Diiodoethane is used as C-X bond formation reagent. It is also used as Pharmaceutical intermediates.
Uses
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.
Purification Methods
Dissolve it in ether, wash it with saturated aqueous Na2S2O3, dry over MgSO4 and evaporate the ether in vacuo and distil it. Store it in the dark. [Molander et al. J Am Chem Soc 109 453 1987]. [Beilstein 1 IV 169.]
1,2-DIIODOETHANESupplier
Tongling LishidaChem Technology Co., Ltd Gold
- Tel
- 0186-06623089 18606623089
- 350737036@qq.com
nantong honglong Gold
- Tel
- 18068950433
- 2516164271@qq.com
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
- Tel
- 021-61259108 18621169109
- market03@meryer.com
3B Pharmachem (Wuhan) International Co.,Ltd.
- Tel
- 821-50328103-801 18930552037
- 3bsc@sina.com
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1,2-DIIODOETHANE(624-73-7)Related Product Information
- 1-Iodobutane
- 1,8-DIIODOOCTANE
- 1,4-Diiodobutane
- 1,7-DIIODOHEPTANE
- 1,3-Diiodopropane
- ETHANE
- VINYL IODIDE
- TETRAFLUORO-1,2-DIIODOETHANE,1,1,2,2-Tetrafluoro-1,2-diiodoethane (stabilized with Copper chip),1,1,2,2-Tetrafluoro-1,2-diiodoethan
- 1,2-DIIODOETHANE
- Iodoethane
- ethylidene iodide
- Iodetryl
- lecithin-bound iodine
- 1,1-diiodoethane
- 3-BROMO-7,8-DIIODO-BICYCLO[4.2.0]OCTA-1,3,5-TRIENE
- PIPERAZINE DIIODIDE
- 1,1-DIIODOETHANE (1,2-14C)
- Quinoline, 8-(1,2-diiodoethylthio)-, diiodide