2,4,6(1H,3H,5H)-Pyrimidinet

Base Information

Chemical Name:2,4,6(1H,3H,5H)-Pyrimidinet
CAS No.:726-79-4
Molecular Formula:C13H18N2O3
Molecular Weight:250.298
Hs Code.:
Mol file:726-79-4.mol

Synonyms:2,4,6(1H,3H,5H)-Pyrimidinet

Suppliers and Price of 2,4,6(1H,3H,5H)-Pyrimidinet

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 4 raw suppliers

Chemical Property of 2,4,6(1H,3H,5H)-Pyrimidinet

Chemical Property:

PSA：57.69000
LogP:1.41930

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2,4,6(1H,3H,5H)-Pyrimidinet

There total 3 articles about 2,4,6(1H,3H,5H)-Pyrimidinet 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:

: 7200-11-5,7245-04-7,7245-06-9,56-29-1
hexabarbital

: 74-88-4
methyl iodide

: 726-79-4
5-(cyclohex-1-en-1-yl)-1,3,5-trimethylpyrimidine-2,4,6(1H,3H,5H)-trione

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
DOI:10.1021/jacs.1c06335

Reference yield:

: 5-(cyclohex-1-en-1-yl)-6-imino-3,5-dimethyldihydropyrimidine-2,4(1H,3H)-dione

: 726-79-4
5-(cyclohex-1-en-1-yl)-1,3,5-trimethylpyrimidine-2,4,6(1H,3H,5H)-trione

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride; water / ethanol / 3 h / Reflux

2: potassium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogenchloride; water; potassium carbonate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jacs.1c06335