Cinchonan-9-one, 6'-methoxy-, (8alpha)-

Base Information

Chemical Name:Cinchonan-9-one, 6'-methoxy-, (8alpha)-
CAS No.:84-31-1
Molecular Formula:C20H22 N2 O2
Molecular Weight:322.407
Hs Code.:2939200050
European Community (EC) Number:201-524-4
UNII:956671AJG7
DSSTox Substance ID:DTXSID70871567
Wikidata:Q27271744
Mol file:84-31-1.mol

Synonyms:6'-methoxycinchonan-9-one;quininone;quininone, (8alpha)-isomer

Suppliers and Price of Cinchonan-9-one, 6'-methoxy-, (8alpha)-

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

TRC
Quininone
2.5g
$ 1940.00

Sigma-Aldrich
Quininone
50mg
$ 1160.00

American Custom Chemicals Corporation
Quininone 95.00%
5MG
$ 503.66

Total 17 raw suppliers

Chemical Property of Cinchonan-9-one, 6'-methoxy-, (8alpha)-

Chemical Property:

Vapor Pressure:2.72E-09mmHg at 25°C
Melting Point:108° (rapid heating)
Refractive Index:1.5700 (estimate)
Boiling Point:477.8°C at 760 mmHg
Flash Point:242.8°C
PSA：42.43000
Density:1.21g/cm³
LogP:3.26040
Water Solubility.:3mg/L(20 oC)
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:322.168127949
Heavy Atom Count:24
Complexity:494

Purity/Quality:

99% ^*data from raw suppliers

Quininone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=CN=C2C=C1)C(=O)C3CC4CCN3CC4C=C
Isomeric SMILES:COC1=CC2=C(C=CN=C2C=C1)C(=O)[C@@H]3C[C@@H]4CCN3C[C@@H]4C=C
Uses Quininone has been shown to have antimalarial activity in mice. Quininone has been shown to aid the binding of drug-induced antibodies to human platelets.

Technology Process of Cinchonan-9-one, 6'-methoxy-, (8alpha)-

There total 13 articles about Cinchonan-9-one, 6'-methoxy-, (8alpha)- 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: 100.0%