Tertatolol

Base Information

Chemical Name:Tertatolol
CAS No.:83688-84-0
Deprecated CAS:34784-64-0
Molecular Formula:C16H25 N O2 S
Molecular Weight:295.446
Hs Code.:2932999099
European Community (EC) Number:280-519-9
UNII:9ZO341YQXP
DSSTox Substance ID:DTXSID80865735
Nikkaji Number:J323.175E
Wikipedia:Tertatolol
Wikidata:Q7705238
NCI Thesaurus Code:C81654
Pharos Ligand ID:WRBUXFBAAWXR
Metabolomics Workbench ID:49702
ChEMBL ID:CHEMBL434200

Synonyms:Artex;Artexal;DL-8-(2'-hydroxy-3'-t-butylaminopropyloxy)thiochroman.HCl;S 2395;S-2395;SE 2395;SE-2395;tertatolol;tertatolol hydrochloride;tertatolol hydrochloride, (+-)-isomer;tertatolol, (+-)-isomer

Suppliers and Price of Tertatolol

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

Usbiological
rac Tertatolol
10mg
$ 460.00

TRC
racTertatolol
10mg
$ 165.00

Medical Isotopes, Inc.
racTertatolol
100 mg
$ 2200.00

Total 7 raw suppliers

Chemical Property of Tertatolol

Chemical Property:

Melting Point:70-72 °C
Boiling Point:465.0±45.0 °C(Predicted)
PKA:13.84±0.20(Predicted)
PSA：66.79000
Density:1.112±0.06 g/cm3(Predicted)
LogP:3.24360
XLogP3:2.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:295.16060021
Heavy Atom Count:20
Complexity:293

Purity/Quality:

98%Min ^*data from raw suppliers

rac Tertatolol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)NCC(COC1=CC=CC2=C1SCCC2)O
Uses 1-(tert-butylamino)-3-[(3,4-dihydro-2H-1-benzothiopyran-8-yl)oxy]propan-2-ol is a benzothiopyran derivative used as an antihypertensive agent. Tertatolol is a β-adrenoceptor blocking agent. Tertatolol is a benzothiopyran derivative used as an antihypertensive agent. Tertatolol is a β-adrenoceptor blocking agent.

Technology Process of Tertatolol

There total 2 articles about Tertatolol 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: