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Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)-

Base Information Edit
  • Chemical Name:Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)-
  • CAS No.:115385-08-5
  • Molecular Formula:C41H54Ge2
  • Molecular Weight:692.06
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40454109
  • Nikkaji Number:J1.163.153C
  • Mol file:115385-08-5.mol
Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)-

Synonyms:Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)-;115385-08-5;DTXSID40454109;1,1,2,2-Tetra(2,6-diethylphenyl)-1,2-digermacyclopropane

Suppliers and Price of Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)-
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
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Total 0 raw suppliers
Chemical Property of Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)- Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:12
  • Exact Mass:692.2658053
  • Heavy Atom Count:43
  • Complexity:595
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=C(C(=CC=C1)CC)[Ge](C[Ge](C2=C(C=CC=C2CC)CC)C3=C(C=CC=C3CC)CC)C4=C(C=CC=C4CC)CC
Technology Process of Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)-

There total 1 articles about Digermirane, 1,1,2,2-tetrakis(2,6-diethylphenyl)- 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 diethyl ether; cyclohexane; byproducts: N2; Irradiation (UV/VIS); Soln. of digermene, prepd. by irradiation of cyclotrigermane at room temp., is transferred to etheral soln. of CH2N2 under Ar at -78°C, mixt. is warmed to room temp.; crystn. (hexane), elem. anal.;
DOI:10.1021/om00098a036
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