Perylene, 3,10-dinitro-

Base Information

Chemical Name:Perylene, 3,10-dinitro-
CAS No.:91997-67-0
Molecular Formula:C₂₀H₁₀N₂O₄
Molecular Weight:342.31
Hs Code.:
DSSTox Substance ID:DTXSID90238810
Wikidata:Q83121141

Synonyms:3,10-Dinitroperylene;Perylene, 3,10-dinitro-;91997-67-0;SCHEMBL7912372;DTXSID90238810

Suppliers and Price of Perylene, 3,10-dinitro-

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 2 raw suppliers

Chemical Property of Perylene, 3,10-dinitro-

Chemical Property:

Vapor Pressure:1.37E-13mmHg at 25°C
Boiling Point:597.1°Cat760mmHg
Flash Point:298°C
PSA：91.64000
Density:1.557g/cm³
LogP:6.60000
XLogP3:5.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:342.06405680
Heavy Atom Count:26
Complexity:548

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C3C(=C1)C(=CC=C3C4=CC=C(C5=CC=CC2=C54)[N+](=O)[O-])[N+](=O)[O-]

Technology Process of Perylene, 3,10-dinitro-

There total 5 articles about Perylene, 3,10-dinitro- 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:

: 198-55-0
PERYLENE

: 91997-67-0
3,10-Dinitroperylene

Guidance literature:: With sulfuric acid; acetic acid; potassium nitrate; at 100 ℃;

Reference yield:

: 198-55-0
PERYLENE

: 91997-67-0
3,10-Dinitroperylene

: 91997-66-9
3,9-Dinitroperylene

: 3,4-Dinitroperylene

Guidance literature:: With nitric acid; In tetrachloromethane; at 20 ℃; for 2h; Title compound not separated from byproducts;
DOI:10.1002/recl.19931121105