9(10H)-Acridinone, 1-hydroxy-2,3-dimethoxy-

Base Information

Chemical Name:9(10H)-Acridinone, 1-hydroxy-2,3-dimethoxy-
CAS No.:17014-43-6
Molecular Formula:C₁₅H₁₃NO₄
Molecular Weight:271.273
Hs Code.:2933990090
DSSTox Substance ID:DTXSID10168807
Nikkaji Number:J13.590I
Wikidata:Q83038422
Mol file:17014-43-6.mol

Synonyms:xanthoxoline

Suppliers and Price of 9(10H)-Acridinone, 1-hydroxy-2,3-dimethoxy-

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

Biosynth Carbosynth
Xanthoxoline
1 mg
$ 125.00

AK Scientific
9(10H)-Acridinone,1-hydroxy-2,3-dimethoxy-
1mg
$ 218.00

Total 3 raw suppliers

Chemical Property of 9(10H)-Acridinone, 1-hydroxy-2,3-dimethoxy-

Chemical Property:

Vapor Pressure:1.02E-09mmHg at 25°C
Melting Point:256-257 °C
Boiling Point:476.9°Cat760mmHg
PKA:7.28±0.20(Predicted)
Flash Point:242.2°C
PSA：71.55000
Density:1.323g/cm³
LogP:2.40410
XLogP3:3.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:271.08445790
Heavy Atom Count:20
Complexity:375

Purity/Quality:

99% ^*data from raw suppliers

Xanthoxoline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=C2C(=C1)NC3=CC=CC=C3C2=O)O)OC
Description Isolated from the leaves of Evodia xanthoxyloides, this alkaloid forms pale yellow crystals which have two melting points with intermediate solidification. Oxidation with concen trated HN03 furnishes 1: 4-dihydro-4-oxo-3-quinoline carboxylic acid while treatment with methyl iodide in the presence of potassium carbonate gives Melicopidine (q.v.).

Technology Process of 9(10H)-Acridinone, 1-hydroxy-2,3-dimethoxy-

There total 2 articles about 9(10H)-Acridinone, 1-hydroxy-2,3-dimethoxy- 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: