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

Base Information

Chemical Name:Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-(4-chlorophenyl)-
CAS No.:152423-16-0
Molecular Formula:C₁₃H₇ClN₄S₂
Molecular Weight:318.81
Hs Code.:
NSC Number:669950
DSSTox Substance ID:DTXSID00165027
Nikkaji Number:J551.030I
Wikidata:Q83034152
ChEMBL ID:CHEMBL1995408

Synonyms:NSC669950;Pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione, 6-(4-chlorophenyl)-;6-(4-Chlorophenyl)pyrazolo(3,4-d)thiazolo(3,2-a)pyrimidine-4(1H)-thione;152423-16-0;C13H7ClN4S2;CHEMBL1995408;C13-H7-Cl-N4-S2;DTXSID00165027;NSC-669950;NCI60_024480;LS-129355;5-(4-Chlorophenyl)-7-thia-4a,8-diazacyclopent[f]indazole-4(1H)-thione;6-(4-chlorophenyl)-1H-pyrazolo[[?]]thiazolo[[?]]pyrimidine-4-thione;6-(4-Chlorophenyl)pyrazolo[3,4-d][1,3]thiazolo[3,2-a]pyrimidine-4(1H)-thione

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

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

Chemical Property:

Vapor Pressure:6.46E-14mmHg at 25°C
Boiling Point:590.4°Cat760mmHg
Flash Point:310.9°C
Density:1.72g/cm³
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:317.9800663
Heavy Atom Count:20
Complexity:499

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1C2=CSC3=NC4=C(C=NN4)C(=S)N23)Cl

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

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

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

: 152423-16-0
6-(4-Chloro-phenyl)-1H-pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidine-4-thione

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / Na₂CO₃ / acetone / 24 h

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

3: 80 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:

: 536-38-9
4-chlorobenzoylmethyl bromide

: 152423-16-0
6-(4-Chloro-phenyl)-1H-pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidine-4-thione

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / Na₂CO₃ / acetone / 24 h

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

3: 80 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:

: 152423-00-2
6-[2-(4-Chloro-phenyl)-2-oxo-ethylsulfanyl]-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one

: 152423-16-0
6-(4-Chloro-phenyl)-1H-pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidine-4-thione

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / conc. aq. sulphuric acid / 120 h

2: 80 percent / Laweson's reagent / xylene / 28 h / Heating

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