1,6,7-Trichloronaphthalene

Base Information

Chemical Name:1,6,7-Trichloronaphthalene
CAS No.:55720-39-3
Molecular Formula:C10H5 Cl3
Molecular Weight:231.51
Hs Code.:
DSSTox Substance ID:DTXSID20204265
Nikkaji Number:J167.207J
Wikidata:Q81977286
Mol file:55720-39-3.mol

Synonyms:1,6,7-Trichloronaphthalene;55720-39-3;Naphthalene, 1,6,7-trichloro;Naphthalene, 1,6,7-trichloro-;DTXSID20204265;FUEZTEBYLIMNHN-UHFFFAOYSA-N

Suppliers and Price of 1,6,7-Trichloronaphthalene

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 3 raw suppliers

Chemical Property of 1,6,7-Trichloronaphthalene

Chemical Property:

Vapor Pressure:0.00053mmHg at 25°C
Boiling Point:322.3°Cat760mmHg
Flash Point:220°C
PSA：0.00000
Density:1.452g/cm³
LogP:4.80000
XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:229.945683
Heavy Atom Count:13
Complexity:183

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=CC(=C(C=C2C(=C1)Cl)Cl)Cl

Technology Process of 1,6,7-Trichloronaphthalene

There total 10 articles about 1,6,7-Trichloronaphthalene 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:

: 55720-43-9
1,4,6,7-tetrachloronaphthalene

: 2437-54-9
1,4,6-trichloronaphthalene

: 55720-39-3
2,3,5-trichloronaphthalene

Guidance literature:: In acetonitrile; Product distribution; Mechanism; Irradiation; addition of triethylamine and/or 1,3-pentadiene;
DOI:10.1016/S0040-4039(00)93535-4