Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-phenyl-

Base Information

Chemical Name:Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-phenyl-
CAS No.:152423-15-9
Molecular Formula:C₁₃H₈N₄S₂
Molecular Weight:284.365
Hs Code.:
DSSTox Substance ID:DTXSID40165026
Nikkaji Number:J551.029E
Wikidata:Q83034150
Mol file:152423-15-9.mol

Synonyms:6-Phenylpyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione;Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-phenyl-;152423-15-9;C13H8N4S2;DTXSID40165026;C13-H8-N4-S2;LS-129358;5-Phenyl-7-thia-4a,8-diazacyclopent[f]indazole-4(1H)-thione

Suppliers and Price of Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-phenyl-

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
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price

Total 1 raw suppliers

Chemical Property of Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-phenyl-

Chemical Property:

Vapor Pressure:3.45E-13mmHg at 25°C
Boiling Point:574.2°Cat760mmHg
Flash Point:301.1°C
Density:1.61g/cm³
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:284.01903862
Heavy Atom Count:19
Complexity:467

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CSC3=NC4=C(C=NN4)C(=S)N23

Technology Process of Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-phenyl-

There total 4 articles about Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-phenyl- 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: 52.0%

: 152423-08-0
6-Phenyl-1H-pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidin-4-one

: 152423-15-9
6-Phenyl-1H-pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidine-4-thione

Guidance literature:: With Lawessons reagent; In xylene; for 28h; Heating;
DOI:10.1016/0223-5234(93)90123-V

Reference yield:

: 24521-76-4
6-thioxo-1,5,6,7-tetrahydropyrazolo<3,4-d>pyrimidin-4-one

: 152423-15-9
6-Phenyl-1H-pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidine-4-thione

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / Na₂CO₃ / acetone / 24 h

2: 90 percent / conc. aq. sulphuric acid / 120 h / Ambient temperature

3: 52 percent / Laweson's reagent / xylene / 28 h / Heating

With Lawessons reagent; sulfuric acid; sodium carbonate; In acetone; xylene;
DOI:10.1016/0223-5234(93)90123-V

Reference yield:

: 70-11-1
α-bromoacetophenone

: 152423-15-9
6-Phenyl-1H-pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidine-4-thione

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / Na₂CO₃ / acetone / 24 h

2: 90 percent / conc. aq. sulphuric acid / 120 h / Ambient temperature

3: 52 percent / Laweson's reagent / xylene / 28 h / Heating

With Lawessons reagent; sulfuric acid; sodium carbonate; In acetone; xylene;
DOI:10.1016/0223-5234(93)90123-V