1-Phenylacenaphthylene

Base Information

Chemical Name:1-Phenylacenaphthylene
CAS No.:4044-56-8
Molecular Formula:C18H12
Molecular Weight:228.293
Hs Code.:
DSSTox Substance ID:DTXSID50519399
Nikkaji Number:J330.545G
Wikidata:Q82382550
Mol file:4044-56-8.mol

Synonyms:1-phenylacenaphthylene;4044-56-8;1-phenyl acenaphthylene;1-phenyl-acenaphthylene;DTXSID50519399

Suppliers and Price of 1-Phenylacenaphthylene

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 1 raw suppliers

Chemical Property of 1-Phenylacenaphthylene

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:228.093900383
Heavy Atom Count:18
Complexity:334

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=CC3=CC=CC4=C3C2=CC=C4

Technology Process of 1-Phenylacenaphthylene

There total 15 articles about 1-Phenylacenaphthylene 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: 80.0%

: 98-88-4
benzoyl chloride

: 208-96-8,25036-01-5
acenaphthylene

: 4044-56-8
1-phenylacenaphthylene

Guidance literature:: bis(ethylene)rhodium(I) chloride dimer; In xylene; for 5h; Heating;
DOI:10.1002/adsc.200404145

Reference yield:

: 100-56-1
phenylmercury(II) chloride

: 208-96-8,25036-01-5
acenaphthylene

: 4044-56-8
1-phenylacenaphthylene

Guidance literature:: With sodium acetate; lithium chloride; palladium dichloride; In acetic acid; Ambient temperature;
DOI:10.1246/bcsj.47.1683