131194-18-8

Basic information

• Product Name: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-[(1Z)-prop-1-en-1-yl]pyrimidine-2,4(1H,3H)-dione
• CAS NO: 131194-18-8
• Molecular Formula: C₁₁H₁₆N₂O₄
• Molecular Weight: 240.2557
• Mol File: 131194-18-8.mol

Chemical Properties

• Density: 1.266g/cm³
• Refractive Index: 1.577
• CAS DataBase Reference: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-[(1Z)-prop-1-en-1-yl]pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-[(1Z)-prop-1-en-1-yl]pyrimidine-2,4(1H,3H)-dione(131194-18-8)
• EPA Substance Registry System: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-[(1Z)-prop-1-en-1-yl]pyrimidine-2,4(1H,3H)-dione(131194-18-8)

Safety Data

• Hazardous Substances Data: 131194-18-8(Hazardous Substances Data)

Usage

Chemical structure

The compound contains a pyrimidine ring with a methyl and propenyl group attached to it, and a hydroxyethoxy methyl group attached to the ring.

Molecular weight

Approximately 240.27 g/mol

Functional groups

The compound has several functional groups, including a pyrimidine ring, a hydroxyl group, an ether group, a methyl group, and a propenyl group.

Stereochemistry

The compound has a (1Z)-prop-1-en-1-yl group, indicating the presence of a double bond with a Z configuration.

Applications

The compound can be used in various applications such as pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis.

Potential biological activity

Due to its unique chemical structure, the compound may have potential biological activity or therapeutic uses. Further research may be needed to fully understand its properties and potential uses.

Solubility

The solubility of the compound in different solvents is not provided in the material, but it can be inferred that it may be soluble in polar solvents like water or methanol due to the presence of the hydroxyl and ether groups.

Stability

The stability of the compound under various conditions (e.g., temperature, pH, light) is not provided in the material, but it is generally expected that such compounds should be stored in a cool, dry, and dark place to maintain their stability.

Reactivity

The reactivity of the compound with other chemicals or under different conditions is not provided in the material. However, it is important to consider the reactivity of the functional groups present in the molecule when handling or synthesizing the compound.

Upstream product

• 131194-15-5 1-<<2-<(tert-butyldimethylsilyl)oxy>ethoxy>methyl>-6-(2-methylethynyl)thymine 
• 121749-93-7 1-<<2-<(tert-butyldimethylsilyl)oxy>ethoxy>methyl>-6-iodothymine 
• 125056-88-4 1-[(2-hydroxyethoxy)methyl]-6-(1-propynyl)thymine 

Relevant articles and documents

6-substituted acyclopyrimidine nucleoside derivatives and antiviral agents containing the same as active ingredient thereof

6-substitutted acyclopyrimidine nucleoside derivatives represented by the following general formula I: STR1 wherein R1 represents a hydrogen or halogen atom or a group of alkyl, alkenyl, alkynyl, alkylcarbonyl, arylcarbonyl, arylcarbonylalkyl,

A new class of HIV-1-specific 6-substituted acyclouridine derivatives: Synthesis and anti-HIV-1 activity of 5- or 6-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)

A series of novel acyclouridine derivatives substituted at both the C-5 and C-6 positions were synthesized for the purpose of improving the activity of a recently reported HIV-1-specific lead, 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT). Prep