5000-33-9 Usage
Description
4-amino-1-(tetrahydro-2H-pyran-2-yl)pyrimidin-2(1H)-one is a pyrimidinone derivative with a molecular formula of C9H14N3O2. It features a tetrahydro-2H-pyran-2-yl group attached to the amino group at the 4-position of the pyrimidine ring. This chemical compound has potential applications in medicinal chemistry, particularly as a scaffold for the development of new drugs. It may also possess biological activities and could be utilized in the study of pyrimidine derivatives and their pharmacological properties. Ongoing research is exploring its potential uses and properties in various fields.
Used in Medicinal Chemistry:
4-amino-1-(tetrahydro-2H-pyran-2-yl)pyrimidin-2(1H)-one is used as a scaffold for the development of new drugs due to its unique structure and potential biological activities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-amino-1-(tetrahydro-2H-pyran-2-yl)pyrimidin-2(1H)-one is used as a compound for studying pyrimidine derivatives and their pharmacological properties, which may lead to the discovery of novel therapeutic agents.
Used in Biological Activity Studies:
4-amino-1-(tetrahydro-2H-pyran-2-yl)pyrimidin-2(1H)-one is used as a subject of research to explore its potential biological activities and understand its role in various biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 5000-33-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5000-33:
(6*5)+(5*0)+(4*0)+(3*0)+(2*3)+(1*3)=39
39 % 10 = 9
So 5000-33-9 is a valid CAS Registry Number.
5000-33-9Relevant articles and documents
A general approach to the synthesis of 5-S-functionalized pyrimidine nucleosides and their analogues
Kananovich, Dzmitry G.,Reino, Alli,Ilmarinen, Kaja,Roomusoks, Marko,Karelson, Mati,Lopp, Margus
, p. 5634 - 5644 (2014/07/22)
A general and efficient approach was developed for the introduction of S-functionality at the C-5 position of cytosine and uracil nucleosides and their analogues. The key step is a palladium-catalyzed C-S coupling of the corresponding 5-bromo nucleoside derivative and alkyl thiol. The butyl 3-mercaptopropionate coupling products were further converted to the corresponding disulphides, the stable precursors of 5-mercaptopyrimidine nucleosides. the Partner Organisations 2014.
