Silane, chlorodimethyl[(trichlorosilyl)methyl]-

Base Information

Chemical Name:Silane, chlorodimethyl[(trichlorosilyl)methyl]-
CAS No.:16538-60-6
Molecular Formula:C3H8Cl4Si2
Molecular Weight:242.08
Hs Code.:
DSSTox Substance ID:DTXSID60451791
Nikkaji Number:J1.862.074J
Wikidata:Q82272014

Synonyms:Silane, chlorodimethyl[(trichlorosilyl)methyl]-;SCHEMBL7556421;DTXSID60451791;GJIIJSWYRBEOCZ-UHFFFAOYSA-N;Chlorodimethylsilyl(trichlorosilyl)methane;16538-60-6;1,1,1,3-tetrachloro-3-methyl-1,3-disilabutane;1,1,1,3-tetrachloro-3,3-dimethyl-(disilylmethane)

Suppliers and Price of Silane, chlorodimethyl[(trichlorosilyl)methyl]-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Silane, chlorodimethyl[(trichlorosilyl)methyl]-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:241.888914
Heavy Atom Count:9
Complexity:96.5

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[Si](C)(C[Si](Cl)(Cl)Cl)Cl

Technology Process of Silane, chlorodimethyl[(trichlorosilyl)methyl]-

There total 1 articles about Silane, chlorodimethyl[(trichlorosilyl)methyl]- 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: 56.0%

: 1440146-75-7
trichloro[[dimethyl(2,4,6-trimethoxyphenyl)silyl]methyl]silane

: 621-23-8
1,2,3-trimethoxybenzene

: 16538-60-6
3-methyl-1,1,1,3-tetrachloro-1,3-disilabutane

Guidance literature:: With hydrogenchloride; In diethyl ether; at 0 - 20 ℃; for 1.83333h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/om400190q