2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-dioxazatrisilinane

Base Information

Chemical Name:2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-dioxazatrisilinane
CAS No.:7418-21-5
Molecular Formula:C6H19NO2Si3
Molecular Weight:221.479
Hs Code.:
DSSTox Substance ID:DTXSID80499377
Wikidata:Q82350106

Synonyms:7418-21-5;2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-dioxazatrisilinane;1,3-Dioxa-5-aza-2,4,6-trisilacyclohexane, 2,2,4,4,6,6-hexamethyl-;DTXSID80499377

Suppliers and Price of 2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-dioxazatrisilinane

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
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price

Total 3 raw suppliers

Chemical Property of 2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-dioxazatrisilinane

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:221.07235845
Heavy Atom Count:12
Complexity:175

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C[Si]1(N[Si](O[Si](O1)(C)C)(C)C)C

Technology Process of 2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-dioxazatrisilinane

There total 1 articles about 2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-dioxazatrisilinane 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: 40.0%

: 3262-89-3
triphenylboroxine

: 1009-93-4
2,2,4,4,6,6-hexamethylcyclotrisilazane

: 541-05-9
Hexamethylcyclotrisiloxane

: 7418-21-5
2,2,4,4,6,6-hexamethyl-1,3-dioxa-5-aza-2,4,6-trisilacyclohexane

: 976-28-3
2,4,6-triphenylborazine

Guidance literature:: In potassium hydroxide; byproducts: CH4, C6H6; heating 0.01mol phenylboric anhydride and 0.01mol cyclotrisilazane and 0.05g (1%) KOH for 4h at 180-280°C; analysis of liquid and gaseous products by GLC; extractn. of residue with C6H6, removal of solvent, recrystn. of triphenylborazine from heptane, elem. anal.;
DOI:10.1007/BF00956370