2-(Benzylsulfanyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one

Base Information

Chemical Name:2-(Benzylsulfanyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one
CAS No.:141763-22-6
Molecular Formula:C₁₂H₉N₃OS₂
Molecular Weight:275.355
Hs Code.:
DSSTox Substance ID:DTXSID10567356
Wikidata:Q82453226
Mol file:141763-22-6.mol

Synonyms:141763-22-6;DTXSID10567356;2-(Benzylsulfanyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one

Suppliers and Price of 2-(Benzylsulfanyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one

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

Total 1 raw suppliers

Chemical Property of 2-(Benzylsulfanyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:275.01870427
Heavy Atom Count:18
Complexity:344

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CSC2=NC3=C(S2)N=CNC3=O

Technology Process of 2-(Benzylsulfanyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one

There total 2 articles about 2-(Benzylsulfanyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one 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:

: 141763-21-5
5-amino-2-benzylmercapto-thiazole-4-carboxylic acid amide

: 141763-22-6
2-benzylmercapto-6H-thiazolo[5,4-d]pyrimidin-7-one

Guidance literature:: With acetic anhydride; orthoformic acid triethyl ester;
DOI:10.1039/jr9490002329

Reference yield:

: 100-44-7
benzyl chloride

: 141763-22-6
2-benzylmercapto-6H-thiazolo[5,4-d]pyrimidin-7-one

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous NaOH

2: orthoformic acid triethyl ester; acetic acid anhydride

With sodium hydroxide; acetic anhydride; orthoformic acid triethyl ester;
DOI:10.1039/jr9490002329