8H-Dibenzo(B,MN)phenanthren-8-one

Base Information

Chemical Name:8H-Dibenzo(B,MN)phenanthren-8-one
CAS No.:28609-66-7
Molecular Formula:C₂₁H₁₂O
Molecular Weight:280.326
Hs Code.:
DSSTox Substance ID:DTXSID20182791
Nikkaji Number:J1.596.456A
Wikidata:Q83053493

Synonyms:8H-DIBENZO(B,MN)PHENANTHREN-8-ONE;28609-66-7;86854-06-0;9H-Dibenz(a,de)anthracen-9-one;DTXSID20182791;9H-Dibenzo[a,de]anthracene-9-one

Suppliers and Price of 8H-Dibenzo(B,MN)phenanthren-8-one

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
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Total 0 raw suppliers

Chemical Property of 8H-Dibenzo(B,MN)phenanthren-8-one

Chemical Property:

Vapor Pressure:7.83E-15mmHg at 25°C
Boiling Point:610.2°Cat760mmHg
Flash Point:274.9°C
Density:1.32g/cm³
XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:280.088815002
Heavy Atom Count:22
Complexity:593

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C3C4=CC=CC(=O)C4=CC5=C3C2=CC=C5

Technology Process of 8H-Dibenzo(B,MN)phenanthren-8-one

There total 8 articles about 8H-Dibenzo(B,MN)phenanthren-8-one 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: 71.0%

: 898821-54-0
2-(9-phenanthryl)benzenecarboxaldehyde

: 28609-66-7
8H-benzo[gh]tetraphen-8-one

: 86853-96-5
13H-indeno[1,2-l]phenanthren-13-one

Guidance literature:: With tetrafluoroboric acid; Barluenga reagent; In diethyl ether; dichloromethane; at 0 - 20 ℃; for 3h;
DOI:10.1002/anie.200504448