2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt

Base Information

Chemical Name:2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt
CAS No.:1431470-08-4
Molecular Formula:BrH*C₁₂H₈BrN₃OS
Molecular Weight:403.097
Hs Code.:

Synonyms:2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt

Suppliers and Price of 2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt

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 0 raw suppliers

Chemical Property of 2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt

There total 2 articles about 2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt 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: 46.0%

: 1431470-41-5
(4-oxo-6-phenyl-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl)carbamic acid tert-butyl ester

: 1431470-08-4
2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt

Guidance literature:: With bromine; In chloroform; at 20 ℃; for 2h;

Reference yield:

: 1216257-25-8
2-amino-6-phenyl-thieno[2,3-d]pyrimidin-4(3H)-one

: 1431470-08-4
2-amino-5-bromo-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one hydrobromide salt

Guidance literature:: Multi-step reaction with 2 steps

1: dmap / N,N-dimethyl-formamide / 18 h / 20 °C

2: bromine / chloroform / 2 h / 20 °C

With dmap; bromine; In chloroform; N,N-dimethyl-formamide;