Thalidasine

Base Information

Chemical Name:Thalidasine
CAS No.:16623-56-6
Molecular Formula:C₃₉H₄₄N₂O₇
Molecular Weight:652.788
Hs Code.:
DSSTox Substance ID:DTXSID801318210
Nikkaji Number:J66.391C
Wikidata:Q27108420
ChEMBL ID:CHEMBL506593
Mol file:16623-56-6.mol

Synonyms:thalidasine

Suppliers and Price of Thalidasine

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

American Custom Chemicals Corporation
THALIDASINE 95.00%
5MG
$ 495.90

Total 2 raw suppliers

Chemical Property of Thalidasine

Chemical Property:

Vapor Pressure:9.29E-22mmHg at 25°C
Melting Point:105-107 °C
Boiling Point:739.9°Cat760mmHg
PKA:7.35±0.20(Predicted)
Flash Point:181.1°C
PSA：71.09000
Density:1.175g/cm³
LogP:7.04680
XLogP3:6.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:5
Exact Mass:652.31485175
Heavy Atom Count:48
Complexity:1030

Purity/Quality:: THALIDASINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC)OC
Isomeric SMILES:CN1CCC2=CC(=C(C3=C2[C@@H]1CC4=CC(=C(C=C4)OC)OC5=CC=C(C[C@H]6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC)OC
Description Thalictrum dasycarpum yields this bisbenzy1isoquino1ine alkaloid which is obtained as an amorphous powder. It has [α]27D- 70° (c 0.89, MeOH) and gives an ultraviolet spectrum with absorption maxima at 275 and 282 IT1J1. The alkaloid yields a crystalline oxalate, m.p. 160-2°C; picrate, m.p. 175-7°C and the methiodide, m.p. 182-3°C. Five methoxyl groups are present and two methylimino groups.

Technology Process of Thalidasine

There total 4 articles about Thalidasine 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: