91233-70-4

Basic information

• Product Name: 5-Pyrimidinol, 2-methoxy- (9CI)
• Synonyms: 5-Pyrimidinol, 2-methoxy- (9CI);5-Hydroxy-2-methoxypyrimidine;2-MethoxypyriMidin-5-ol;2-methoxy-5-Pyrimidinol;2-Methoxypyrimidine-5-ol
• CAS NO: 91233-70-4
• Molecular Formula: C₅H₆N₂O₂
• Molecular Weight: 126.11334
• Product Categories: PYRIMIDINE
• Mol File: 91233-70-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 282.3 °C at 760 mmHg
• Flash Point: 124.6 °C
• Appearance: /
• Density: 1.282g/cm³
• Vapor Pressure: 0.00198mmHg at 25°C
• Refractive Index: 1.543
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 5-Pyrimidinol, 2-methoxy- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Pyrimidinol, 2-methoxy- (9CI)(91233-70-4)
• EPA Substance Registry System: 5-Pyrimidinol, 2-methoxy- (9CI)(91233-70-4)

Safety Data

• Hazardous Substances Data: 91233-70-4(Hazardous Substances Data)

Usage

General Description

5-Pyrimidinol, 2-methoxy- (9CI) is a chemical compound with the molecular formula C5H6N2O2. It is a pyrimidine derivative with a methoxy group attached to the 2-position of the pyrimidinol ring. 5-Pyrimidinol, 2-methoxy- (9CI) is used in the synthesis of pharmaceuticals and agrochemicals, and it also has potential applications in organic and medicinal chemistry. Its structure and properties make it a valuable building block for the development of new compounds with potential biological activity. Further research and exploration of 5-Pyrimidinol, 2-methoxy- (9CI) could lead to the discovery of new drugs or agrochemicals with important industrial and medical applications.

InChI:InChI=1/C5H6N2O2/c1-9-5-6-2-4(8)3-7-5/h2-3,8H,1H3

Upstream product

• 628692-15-9 (2-methoxypyrimidin-5-yl)boronic acid 
• 931-63-5 2-methoxypyrimidine 

Relevant articles and documents

C70 Fullerene-Catalyzed Metal-Free Photocatalytic ipso-Hydroxylation of Aryl Boronic Acids: Synthesis of Phenols

A metal-free C70 fullerene-catalyzed method has been developed for the ipso-hydroxylation of aryl and heteroaryl boronic acids to corresponding phenols under photocatalytic conditions. The reaction proceeds under oxygen atmosphere and the mechanistic study revealed that C70 plays a critical role in the generation of reactive oxygen species in the presence of blue light. Reactions in the presence of 18O-labelled water and oxygen confirmed the generation of reactive oxygen species from oxygen molecule. Amine used as a reductant could be recovered in the form of imine. The current method is also applicable to the synthesis of aryl ethers in one-pot two-step process. (Figure presented.).