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Germane, triethylphenyl-

Base Information Edit
  • Chemical Name:Germane, triethylphenyl-
  • CAS No.:2817-41-6
  • Molecular Formula:C12H20Ge
  • Molecular Weight:236.881
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00460206
  • Nikkaji Number:J1.345.372A
  • Wikidata:Q82284180
  • Mol file:2817-41-6.mol
Germane, triethylphenyl-

Synonyms:Germane, triethylphenyl-;Phenyltriethylgermane;2817-41-6;DTXSID00460206

Suppliers and Price of Germane, triethylphenyl-
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Germane, triethylphenyl- Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:4
  • Exact Mass:238.0776784
  • Heavy Atom Count:13
  • Complexity:124
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC[Ge](CC)(CC)C1=CC=CC=C1
Technology Process of Germane, triethylphenyl-

There total 11 articles about Germane, triethylphenyl- 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:
With phenylmagnesium bromide; In diethyl ether; benzene; addn. of the germane in benzene to the freshly prepd. Grignard compoundin ether; refluxing for 3.5 h;; hydrolized with ice and dilute hydrochloric acid; chromy. (silica gel, hexane); fractional distn.;;
DOI:10.1246/bcsj.59.2807
Guidance literature:
In methanol; at room temp. 4 days; hydrolysis of reaction mixture; detected by GC-MS and NMR;
DOI:10.1246/cl.2001.1086
Guidance literature:
With magnesium; In tetrahydrofuran; byproducts: MgBr2; Sonication; the mixt. of magnesium, germane and halogen-compound in THF was sonicated for 2 h (inert atm.); the mixt. was washed with satd. soln. of NaCl, extd. with diethyl ether,the organic layer was dried over MgSO4, the solvent was removed under r educed pressure, column chromy. (petroleum ether-diethyl ether 95/5);
DOI:10.1016/S0022-328X(03)00053-6
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