Methylademecolcine, N-

Base Information

Chemical Name:Methylademecolcine, N-
CAS No.:7336-44-9
Molecular Formula:C₂₂H₂₇NO₅
Molecular Weight:385.46
Hs Code.:
NSC Number:403150
DSSTox Substance ID:DTXSID10223607
Nikkaji Number:J71.260D
Wikidata:Q83102069
Metabolomics Workbench ID:143529
ChEMBL ID:CHEMBL88003
Mol file:7336-44-9.mol

Synonyms:N-Methylcolchamine;Methylademecolcine, N-;Demecolcine, N-methyl-;N-Methyldemecolcine;7336-44-9;N-Deacetyl-N,N-dimethylcolchicine;B631861F037K145;COLCHICINE, N-DEACETYL-N,N-DIMETHYL-;NSC 403150;Benzo(a)heptalen-9(5H)-one, 7-dimethylamino-6,7-dihydro-1,2,3,10-tetramethoxy-, (S)-;NSC403150;CHEMBL88003;DTXSID10223607;NSC-403150;LS-54674

Suppliers and Price of Methylademecolcine, N-

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 5 raw suppliers

Chemical Property of Methylademecolcine, N-

Chemical Property:

Vapor Pressure:2.76E-15mmHg at 25°C
Melting Point:206-8°C
Boiling Point:619.7°C at 760 mmHg
Flash Point:328.6°C
PSA：57.23000
Density:1.2g/cm³
LogP:3.29710
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:385.18892296
Heavy Atom Count:28
Complexity:680

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC
Isomeric SMILES:CN(C)[C@H]1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC
Description A colchicine type alkaloid, N-methylcolchamine occurs in Merendera robusta Bge. It is laevorotatory having a specific rotation of [α]D - 109° (CHC13). The structure has been established from spectroscopic data and by comparison with colchamine.

Technology Process of Methylademecolcine, N-

There total 3 articles about Methylademecolcine, N- 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: