Terosite

Base Information

Chemical Name:Terosite
CAS No.:24368-63-6
Molecular Formula:C33H23 N3
Molecular Weight:461.5558
Hs Code.:
DSSTox Substance ID:DTXSID10179110
Nikkaji Number:J1.457.468I
Wikidata:Q83049625
Mol file:24368-63-6.mol

Synonyms:2,6-bis(4-phenyl-2-pyridyl)-4-phenylpyridine;terosite

Suppliers and Price of Terosite

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 0 raw suppliers

Chemical Property of Terosite

Chemical Property:

Boiling Point:624°Cat760mmHg
Flash Point:263.8°C
PSA：38.67000
Density:1.166g/cm³
LogP:8.20660
XLogP3:7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:461.189197746
Heavy Atom Count:36
Complexity:601

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC(=NC=C2)C3=CC(=CC(=N3)C4=NC=CC(=C4)C5=CC=CC=C5)C6=CC=CC=C6

Technology Process of Terosite

There total 3 articles about Terosite 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:

: 52565-58-9
1-(4-phenylpyridin-2-yl)ethan-1-one

: 100-52-7
benzaldehyde

: 24368-63-6
4,4',4''-triphenyl-2,2':6',2''-terpyridine

Guidance literature:: With ammonium acetate; ammonium hydroxide; at 250 ℃;
DOI:10.1021/ja01603a036

Reference yield:

: 939-23-1
p-phenylpyridine

: 100-52-7
benzaldehyde

: 24368-63-6
4,4',4''-triphenyl-2,2':6',2''-terpyridine

Guidance literature:: With ammonium acetate; sodium ethanolate; Yield given. Multistep reaction; 2.) acetic acid, reflux, 4 h;
DOI:10.1039/DT9910003157