Thiazolo[5,4-d]pyrimidin-7(4H)-one, 2-methyl-

Base Information

Chemical Name:Thiazolo[5,4-d]pyrimidin-7(4H)-one, 2-methyl-
CAS No.:5021-51-2
Molecular Formula:C6H5N3OS
Molecular Weight:167.18800
Hs Code.:

Synonyms:7-Hydroxy-2-methyl-thiazolo<5.4-d>pyrimidin;2-Methyl-thiazolo[5,4-d]pyrimidin-7-ol;2-Methyl-thiazolo<5.4-d>pyrimidin-7-ol;

Suppliers and Price of Thiazolo[5,4-d]pyrimidin-7(4H)-one, 2-methyl-

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

Crysdot
2-Methylthiazolo[5,4-d]pyrimidin-7-ol 97%
10g
$ 1736.00

Crysdot
2-Methylthiazolo[5,4-d]pyrimidin-7-ol 97%
5g
$ 1240.00

Crysdot
2-Methylthiazolo[5,4-d]pyrimidin-7-ol 97%
1g
$ 545.00

Total 4 raw suppliers

Chemical Property of Thiazolo[5,4-d]pyrimidin-7(4H)-one, 2-methyl-

Chemical Property:

Melting Point:None °C
PSA：87.14000
LogP:1.10030

Purity/Quality:

95% ^*data from raw suppliers

2-Methylthiazolo[5,4-d]pyrimidin-7-ol 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Thiazolo[5,4-d]pyrimidin-7(4H)-one, 2-methyl-

There total 9 articles about Thiazolo[5,4-d]pyrimidin-7(4H)-one, 2-methyl- 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:

: 5021-62-5
2-acetylamino-thiomalonamide

: 5021-51-2
2-Methyl-thiazolo<5.4-d>pyrimidin-7-ol

Guidance literature:: Multi-step reaction with 3 steps

1: Heating

2: aq. HCl / Heating

3: acetic anhydride / Heating

With hydrogenchloride; In acetic anhydride;
DOI:10.1248/cpb.13.1319

Reference yield:

: 14056-39-4
acetylaminocyanoacetamide

: 5021-51-2
2-Methyl-thiazolo<5.4-d>pyrimidin-7-ol

Guidance literature:: Multi-step reaction with 4 steps

1: H₂S, aq. NH₃

2: Heating

3: aq. HCl / Heating

4: acetic anhydride / Heating

With hydrogenchloride; ammonium hydroxide; hydrogen sulfide; In acetic anhydride;
DOI:10.1248/cpb.13.1319

Reference yield:

: 118767-93-4
7-chloro-2-methyloxazolo[5,4-d]pyrimidine

: 5021-51-2
2-Methyl-thiazolo<5.4-d>pyrimidin-7-ol

Guidance literature:: Multi-step reaction with 2 steps

1: H₂S, aq. NaOH / ethanol

2: aq. HCl

With hydrogenchloride; sodium hydroxide; hydrogen sulfide; In ethanol;