89943-36-2

Basic information

• Product Name: 5-(EthoxyMethyl)-4(3H)-pyriMidinone
• Synonyms: 5-(EthoxyMethyl)-4(3H)-pyriMidinone;ZIRWIOYGAAZKJB-UHFFFAOYSA-N
• CAS NO: 89943-36-2
• Molecular Formula: C7H10N2O2
• Molecular Weight: 154.1665
• Mol File: 89943-36-2.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer
• Solubility: DMSO (Slightly), Methanol (Slightly, Heated)
• CAS DataBase Reference: 5-(EthoxyMethyl)-4(3H)-pyriMidinone(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(EthoxyMethyl)-4(3H)-pyriMidinone(89943-36-2)
• EPA Substance Registry System: 5-(EthoxyMethyl)-4(3H)-pyriMidinone(89943-36-2)

Safety Data

• Hazardous Substances Data: 89943-36-2(Hazardous Substances Data)

Usage

Description

5-(EthoxyMethyl)-4(3H)-pyriMidinone is a substituted pyrimidine compound that serves as an intermediate in the synthesis of Thiamine (T344185) analogues. It is characterized by the presence of an ethoxymethyl group attached to the 5th position of the pyrimidine ring, which contributes to its unique chemical properties and potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
5-(EthoxyMethyl)-4(3H)-pyriMidinone is used as a key intermediate in the synthesis of Thiamine (T344185) analogues for the development of new pharmaceutical compounds. Thiamine, also known as vitamin B1, plays a crucial role in energy production and cellular metabolism. The analogues synthesized using this intermediate may exhibit modified properties, such as increased stability, enhanced bioavailability, or improved therapeutic effects, making them valuable for the treatment of various diseases and conditions.
Used in Chemical Research:
5-(EthoxyMethyl)-4(3H)-pyriMidinone is also used as a research compound in the field of organic chemistry. Its unique structure and reactivity make it an interesting subject for studying the synthesis, properties, and potential applications of substituted pyrimidines. Researchers can use this compound to explore new reaction pathways, develop novel synthetic methods, or investigate the biological activity of related compounds.