Melicopicine

Base Information

Chemical Name:Melicopicine
CAS No.:517-73-7
Molecular Formula:C18H19 N O5
Molecular Weight:329.353
Hs Code.:2933990090
European Community (EC) Number:208-244-1
NSC Number:402921
UNII:4UCL445ULN
DSSTox Substance ID:DTXSID2075429
Nikkaji Number:J11.812E
Wikidata:Q27107315
Metabolomics Workbench ID:68064
ChEMBL ID:CHEMBL455628
Mol file:517-73-7.mol

Synonyms:melicopicine

Suppliers and Price of Melicopicine

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
Melicopicene
5 mg
$ 100.00

Biosynth Carbosynth
Melicopicene
2 mg
$ 50.00

Total 9 raw suppliers

Chemical Property of Melicopicine

Chemical Property:

Vapor Pressure:1.13E-10mmHg at 25°C
Boiling Point:514°Cat760mmHg
Flash Point:264.6°C
PSA：58.92000
Density:1.221g/cm³
LogP:2.72610
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:329.12632271
Heavy Atom Count:24
Complexity:459

Purity/Quality:

98%min ^*data from raw suppliers

Melicopicene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=CC=CC=C2C(=O)C3=C1C(=C(C(=C3OC)OC)OC)OC

Technology Process of Melicopicine

There total 1 articles about Melicopicine 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:

: 875838-58-7
N-(2,3,4,5-tetramethoxy-phenyl)-anthranilic acid

: 517-73-7
melicopine

Guidance literature:: With trichlorophosphate; Erwaermen des Reaktionsprodukts mit Natriummethylat in Methanol und Erhitzen des Reaktionsprodukts mit Methyljodid;