Tiodazosin

Base Information

Chemical Name:Tiodazosin
CAS No.:66969-81-1
Molecular Formula:C18H21N7O4S
Molecular Weight:431.4688
Hs Code.:
UNII:FQI0PYJ799
DSSTox Substance ID:DTXSID90217180
Nikkaji Number:J19.134E
Wikipedia:Tiodazosin
Wikidata:Q15634026
NCI Thesaurus Code:C72926
ChEMBL ID:CHEMBL2107039
Mol file:66969-81-1.mol

Synonyms:4-amino-6,7-dimethoxy-2-4-(5-methylthio-1,3,4-oxadiazole-2-carbonyl)piperazin-1-yl quinazoline;BL 5111;BL 5111A;tiodazosin;tiodazosin monohydrochloride

Suppliers and Price of Tiodazosin

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

CSNpharm
Tiodazosin
10mg
$ 3679.00

CSNpharm
Tiodazosin
1mg
$ 1437.00

American Custom Chemicals Corporation
TIODAZOSIN 95.00%
5MG
$ 501.05

Total 10 raw suppliers

Chemical Property of Tiodazosin

Chemical Property:

Vapor Pressure:6.68E-19mmHg at 25°C
Boiling Point:690.2°Cat760mmHg
PKA:6.52±0.50(Predicted)
Flash Point:371.2°C
PSA：158.03000
Density:1.5g/cm³
LogP:1.88060
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:5
Exact Mass:431.13757335
Heavy Atom Count:30
Complexity:597

Purity/Quality:

97% ^*data from raw suppliers

Tiodazosin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C2C(=C1)C(=NC(=N2)N3CCN(CC3)C(=O)C4=NN=C(O4)SC)N)OC
Uses Tiodazosin, is a potent competitive postsynaptic alpha adrenergic receptor antagonist.

Technology Process of Tiodazosin

There total 2 articles about Tiodazosin 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: