1,3-Bis(triphenylsilyl)benzene

Base Information Edit

Chemical Name:1,3-Bis(triphenylsilyl)benzene
CAS No.:18920-16-6
Molecular Formula:C42H34Si2
Molecular Weight:594.903
Hs Code.:
European Community (EC) Number:633-772-8
DSSTox Substance ID:DTXSID30402250
Nikkaji Number:J2.124.118K
Wikidata:Q72447610
Mol file:18920-16-6.mol

Synonyms:1,3-bis(triphenylsilyl)benzene;18920-16-6;Triphenyl-(3-triphenylsilylphenyl)silane;UGH-3;M-BIS(TRIPHENYLSILYL)BENZENE;Benzene, 1,3-bis(triphenylsilyl)-;N,N'-Dicarbazolyl-3,5-benzene;DTXSID30402250;MFCD00092866;AKOS024432987;1,3-Bis(triphenylsilyl)benzene, 97%

Suppliers and Price of 1,3-Bis(triphenylsilyl)benzene

Supply Marketing:Edit

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

American Custom Chemicals Corporation
1,3-BIS(TRIPHENYLSILYL)BENZENE 95.00%
5MG
$ 498.26

Total 25 raw suppliers

Chemical Property of 1,3-Bis(triphenylsilyl)benzene Edit

Chemical Property:

Melting Point:345-349℃
PSA：0.00000
Density:1.15
LogP:4.44140
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:8
Exact Mass:594.21990415
Heavy Atom Count:44
Complexity:671

Purity/Quality:

98% ^*data from raw suppliers

1,3-BIS(TRIPHENYLSILYL)BENZENE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36
Safety Statements: 26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC(=CC=C4)[Si](C5=CC=CC=C5)(C6=CC=CC=C6)C7=CC=CC=C7
Uses This material can be used as an ultrahigh energy gap hosts in Deep Blue Organic Electrophosphorescent Devices

Technology Process of 1,3-Bis(triphenylsilyl)benzene

There total 3 articles about 1,3-Bis(triphenylsilyl)benzene 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%

: 76-86-8
Triphenylsilyl chloride

: 108-36-1
1,3-dibromobenzene

: 18920-16-6
hexa-Si-phenyl-Si,Si'-m-phenylene-bis-silane

Guidance literature:: 1,3-dibromobenzene; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Inert atmosphere;

Triphenylsilyl chloride; In tetrahydrofuran; hexane; at -78 - 20 ℃; Inert atmosphere;