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9,12-Diiodo-o-carborane

Base Information Edit
  • Chemical Name:9,12-Diiodo-o-carborane
  • CAS No.:17702-35-1
  • Molecular Formula:C2H10 B10 I2
  • Molecular Weight:396.02
  • Hs Code.:
  • Mol file:17702-35-1.mol
9,12-Diiodo-o-carborane

Synonyms:9,12-Diiodo-closo-1,2-dicarbadodecaborane(12);9,12-Diiodo-o-carborane; closo-9,12-Diiodo-1,2-dicarbadodecaborane(12)

Suppliers and Price of 9,12-Diiodo-o-carborane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Biosynth Carbosynth
  • 9,12-Diiodo-1,2-carborane
  • 5 g
  • $ 2500.00
Total 0 raw suppliers
Chemical Property of 9,12-Diiodo-o-carborane Edit
Chemical Property:
  • PSA:0.00000 
  • LogP:-3.76960 
Purity/Quality:

9,12-Diiodo-1,2-carborane *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 9,12-Diiodo-o-carborane

There total 15 articles about 9,12-Diiodo-o-carborane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In neat (no solvent); (under N2); tube charged with B-compound and I2 under vac., cooled to liq. N2 temp., sealed, heated to 120°C for 30 min, maintained for 2.5 h, slowly cooled to room temp.; sublimed at 50°C under reduced pressure;
DOI:10.1021/ic800362z
Guidance literature:
With aluminium trichloride; iodine; In diethyl ether; dichloromethane; water; mixt. of o-carborane, iodine and AlCl3 in CH2Cl2 gently refluxed for 4 h; iodine added slowly to this mixt., after the reaction was completed, mixt. is stirred at 45°C for an additional 14 h; mixt. poured into ice-cold water, org. layer sepd.; water layer extd. with ether, org. layer washed with 50% aq. Na2CO3 and distilled water and dried over MgSO4; solvent removed under vac.; recrystn. from a 6:1 hexane:CHCl3 mixt.;
Guidance literature:
aluminium trichloride; In dichloromethane; N2-atmosphere, 2 equiv. I2, refluxing for 14 h; pouring in ice-cold water, sepn. of org. layer, extn. of aq. layer (Et2O), washing of org. phases (aq. Na2S2O3, water), drying (MgSO4), evapn.,recrystn. (CH2Cl2);
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