1,3-Bis(trimethylgermyl)-2lambda~4~-diazathia-1,2-diene

Base Information

Chemical Name:1,3-Bis(trimethylgermyl)-2lambda~4~-diazathia-1,2-diene
CAS No.:82587-41-5
Molecular Formula:C₆H₁₈Ge₂N₂S
Molecular Weight:295.468
Hs Code.:
DSSTox Substance ID:DTXSID10586744
NSC Number:353178
Wikidata:Q82478933

Synonyms:82587-41-5;1,3-Bis(trimethylgermyl)-2lambda~4~-diazathia-1,2-diene;DTXSID10586744;NSC353178;NSC-353178

Suppliers and Price of 1,3-Bis(trimethylgermyl)-2lambda~4~-diazathia-1,2-diene

Supply Marketing:

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

Total 2 raw suppliers

Chemical Property of 1,3-Bis(trimethylgermyl)-2lambda~4~-diazathia-1,2-diene

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:295.9623233
Heavy Atom Count:11
Complexity:160

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C[Ge](C)(C)N=S=N[Ge](C)(C)C

Technology Process of 1,3-Bis(trimethylgermyl)-2lambda~4~-diazathia-1,2-diene

There total 1 articles about 1,3-Bis(trimethylgermyl)-2lambda~4~-diazathia-1,2-diene 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:

Reference yield: 35.0%

: 18428-81-4
trithiazyl trichloride

: 41990-70-9
Bis--amin

: 82587-41-5
bis(trimethylgermyl)sulfur diimide

: 1529-47-1
chlorotrimethylgermane

Guidance literature:: With triethylamine; In tetrachloromethane; under N2, N3S3Cl3 in to 50°C warmed CCl4 was added dropwise to Ge-compd. and triethylamine in CCl4 at room temp. with stirring, stirred for 20 h; filtrated, concd. (vacuum, 20 mbar), distd. (0.17 mbar): first Ge(CH3)3Cl then (CH3)3GeNSNGe(CH3)3; elem. anal.;