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1,1,1-Tris(2,4,6-trimethylphenyl)germanamine

Base Information Edit
  • Chemical Name:1,1,1-Tris(2,4,6-trimethylphenyl)germanamine
  • CAS No.:139925-54-5
  • Molecular Formula:C27H35GeN
  • Molecular Weight:446.172
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60587266
  • Wikidata:Q82479661
  • Mol file:139925-54-5.mol
1,1,1-Tris(2,4,6-trimethylphenyl)germanamine

Synonyms:trimesitylgermylamine;139925-54-5;1,1,1-Tris(2,4,6-trimethylphenyl)germanamine;DTXSID60587266

Suppliers and Price of 1,1,1-Tris(2,4,6-trimethylphenyl)germanamine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of 1,1,1-Tris(2,4,6-trimethylphenyl)germanamine Edit
Chemical Property:
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:447.1981279
  • Heavy Atom Count:29
  • Complexity:437
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C(=C1)C)[Ge](C2=C(C=C(C=C2C)C)C)(C3=C(C=C(C=C3C)C)C)N)C
Technology Process of 1,1,1-Tris(2,4,6-trimethylphenyl)germanamine

There total 3 articles about 1,1,1-Tris(2,4,6-trimethylphenyl)germanamine 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 n-butyllithium; In tetrahydrofuran; hexane; byproducts: LiCl; addn. of n-BuLi in hexane to dry NH3 in abs. THF at -30°C (inert gas), addn. of the Ge compd. in THF at room temp.; stored at 20°C for 48 h; evapn., addn. of benzene, filtn. (LiCl) and evapn.;
Guidance literature:
In diethyl ether; byproducts: NaCl; addn. of the Ge compd. in abs. ether to NaNH2 in ether (inert gas), cooling to -80°C and addn. of dry NH3, warmimg to room temp. (within 20 h); addn. of abs. benzene, filtn. and evapn. (vac.); elem. anal.;
Guidance literature:
In tetrahydrofuran; byproducts: LiCl; 20°C;
DOI:10.1016/0022-328X(92)83032-D
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