1,2,4,5-Tetraphenylbenzene

Base Information

Chemical Name:1,2,4,5-Tetraphenylbenzene
CAS No.:3383-32-2
Molecular Formula:C30H22
Molecular Weight:382.505
Hs Code.:
NSC Number:118945
DSSTox Substance ID:DTXSID80297890
Nikkaji Number:J786.882K
Wikidata:Q82039386

Synonyms:1,2,4,5-tetraphenylbenzene;3383-32-2;1,2,4,5-tetraphenylbenzol;NSC118945;2,3,5,6-tetraphenylbenzene;DTXSID80297890;NSC-118945;A937498

Suppliers and Price of 1,2,4,5-Tetraphenylbenzene

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 6 raw suppliers

Chemical Property of 1,2,4,5-Tetraphenylbenzene

Chemical Property:

Vapor Pressure:5.86E-10mmHg at 25°C
Boiling Point:508.5°C at 760 mmHg
Flash Point:261.4°C
Density:1.091g/cm³
XLogP3:9.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:4
Exact Mass:382.172150702
Heavy Atom Count:30
Complexity:394

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC(=C(C=C2C3=CC=CC=C3)C4=CC=CC=C4)C5=CC=CC=C5

Technology Process of 1,2,4,5-Tetraphenylbenzene

There total 11 articles about 1,2,4,5-Tetraphenylbenzene 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: 61.0%

: 13074-99-2
1,2,4,5-tetrachloro-3,6-dibromobenzene

: phenylmagnesium bromide

: 95-94-3
1,2,4,5-tetrachlorobenzene

: 3383-32-2
1,2,4,5-tetraphenylbenzol

Guidance literature:: In tetrahydrofuran; for 16h; Ambient temperature;
DOI:10.1021/jo00350a018

Reference yield: 56.0%

: bis[(η(4)-cycloocta-1,5-diene)(μ-methylene)iridium]

: 501-65-5
diphenyl acetylene

: (C₈H₁₂)IrC₅H(C₆H₅)4

: bis(η4-cyclooctadiene)(μ-methylene)(μ-η1,η3-1,2-diphenylallyl)diiridium

: [(C₈H₁₂)IrC₂(C₆H₅)2]2

: 992-04-1
hexaphenylbenzene

: 3383-32-2
1,2,4,5-tetraphenylbenzol

Guidance literature:: In hexane; under protective gas, to suspn. of Ir complex in n-hexane added at 20°C with stirring C2Ph2, allowed to stand for ca. 15 h; concd., chromd. (Al2O3/5% H2O, at -10°C, n-hexane), concd., crystd. at -78°C; elem. anal.;
DOI:10.1016/S0022-328X(00)86761-3