N-(Formyldeacetyl)thiocolchicine

Base Information

Chemical Name:N-(Formyldeacetyl)thiocolchicine
CAS No.:2731-23-9
Molecular Formula:C₂₁H₂₃NO₅S
Molecular Weight:401.483
Hs Code.:
European Community (EC) Number:807-676-3
DSSTox Substance ID:DTXSID601116472
Nikkaji Number:J1.028.556I
ChEMBL ID:CHEMBL279958

Synonyms:NSC 373031;BRN 2786590;N-(Formyldeacetyl)thiocolchicine;N-Deacetyl-N-formyl-10-thiocolchicine;COLCHICINE, N-DEACETYL-N-FORMYL-10-THIO-;4-14-00-00955 (Beilstein Handbook Reference);7-Demethylthiocholchicine;CHEMBL279958;DTXSID601116472;LS-54677;N-[(7S)-5,6,7,9-Tetrahydro-1,2,3-trimethoxy-10-(methylthio)-9-oxobenzo[a]heptalen-7-yl]formamide

Suppliers and Price of N-(Formyldeacetyl)thiocolchicine

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 2 raw suppliers

Chemical Property of N-(Formyldeacetyl)thiocolchicine

Chemical Property:

Vapor Pressure:1.72E-20mmHg at 25°C
Boiling Point:718.4°Cat760mmHg
Flash Point:388.3°C
Density:1.29g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:401.12969401
Heavy Atom Count:28
Complexity:701

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=C2C(=C1)CCC(C3=CC(=O)C(=CC=C32)SC)NC=O)OC)OC
Isomeric SMILES:COC1=C(C(=C2C(=C1)CC[C@@H](C3=CC(=O)C(=CC=C32)SC)NC=O)OC)OC

Technology Process of N-(Formyldeacetyl)thiocolchicine

There total 2 articles about N-(Formyldeacetyl)thiocolchicine 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: 66.5%