1(4H)-Naphthalenone, 8-amino-2,3,6-tribromo-5-hydroxy-4-imino-

Base Information

Chemical Name:1(4H)-Naphthalenone, 8-amino-2,3,6-tribromo-5-hydroxy-4-imino-
CAS No.:72918-29-7
Molecular Formula:C₁₀H₅Br₃N₂O₂
Molecular Weight:424.874
Hs Code.:2925290090
DSSTox Substance ID:DTXSID5072648
Nikkaji Number:J447.253E
Wikidata:Q82000797
Mol file:72918-29-7.mol

Synonyms:72918-29-7;1(4H)-Naphthalenone, 8-amino-2,3,6-tribromo-5-hydroxy-4-imino-;2,3,7-Tribromo-5-amino-8-hydroxy-1,4-naphthoquinone-1-imine;C10H5Br3N2O2;DTXSID5072648;C10-H5-Br3-N2-O2;8-Amino-2,3,6-tribromo-5-hydroxy-4-imino-1(4H)-naphthalenone

Suppliers and Price of 1(4H)-Naphthalenone, 8-amino-2,3,6-tribromo-5-hydroxy-4-imino-

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(4H)-Naphthalenone, 8-amino-2,3,6-tribromo-5-hydroxy-4-imino-

Chemical Property:

Vapor Pressure:0.000593mmHg at 25°C
Boiling Point:310.6°C at 760 mmHg
Flash Point:141.7°C
PSA：86.18000
Density:2.48g/cm³
LogP:3.25820
XLogP3:3.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:423.78807
Heavy Atom Count:17
Complexity:424

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C2=C(C(=C1Br)O)C(=N)C(=C(C2=O)Br)Br)N

Technology Process of 1(4H)-Naphthalenone, 8-amino-2,3,6-tribromo-5-hydroxy-4-imino-

There total 1 articles about 1(4H)-Naphthalenone, 8-amino-2,3,6-tribromo-5-hydroxy-4-imino- 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: