70291-89-3

Basic information

• Product Name: 2,4(1H,3H)-Pyrimidinedione, 5-(phenylseleno)-
• CAS NO: 70291-89-3
• Molecular Formula: C10H8N2O2Se
• Molecular Weight: 267.146
• Mol File: 70291-89-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2,4(1H,3H)-Pyrimidinedione, 5-(phenylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 5-(phenylseleno)-(70291-89-3)
• EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 5-(phenylseleno)-(70291-89-3)

Safety Data

• Hazardous Substances Data: 70291-89-3(Hazardous Substances Data)

Upstream product

• 1666-13-3 diphenyl diselenide 
• 66-22-8 uracil 
• 645-96-5 Benzeneselenol 
• 696-07-1 5-iodouracil 
• 1820-81-1 5-chlorouracil 
• 51-21-8 5-fluorouracil 

Relevant articles and documents

Phenylselenenyl- and Phenylthio-Substituted Pyrimidines as Inhibitors of Dihydrouracil Dehydrogenase and Uridine Phosphorylase

Lithiation of 5-bromo-2,4-bis(benzyloxy)pyrimidine (3) with n-BuLi at -80 deg C followed by the addition of diphenyl diselenide or diphenyl disulfide as an electrophile furnished the corresponding 5-(phenylhetera)-2,4-bis(benzyloxy)pyrimidine, which on ex

Electrochemical Synthesis of 5-Selenouracil Derivatives by Selenylation of Uracils

A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5-selenouracils has been developed. This transformation was performed in the transition metal-free, oxidant-free, and aerobic conditions, providing a rapid and practical protocol to 5-selenouracil derivatives.

A NaI/H2O2-Mediated Sulfenylation and Selenylation of Unprotected Uracil and Its Derivatives

An efficient iodide-catalyzed/hydrogen peroxide mediated sulfenylation and selenylation of unprotected uracil and its derivatives with simple thiols and diselenides was established. This coupling tolerates a broad variety of functional groups to provide d