Description

5-(2-Methoxybenzylidene)-1,3-Dimethylpyrimidine-2,4,6(1H,3H,5H)-Trione is a specialized barbiturate derivative, a class of compounds known for their significant role in medicinal chemistry and organic synthesis. This compound matters as a versatile chemical intermediate, enabling the development of novel pharmacologically active molecules and advanced materials. Pharmaceutical R&D laboratories, agrochemical manufacturers, and fine chemical producers need this high-purity building block for synthesizing new compounds with potential biological activity.

Application

• Pharmaceutical Intermediate: Key building block in the research and synthesis of novel barbiturate analogs and central nervous system (CNS) active compounds.
• Agrochemical Research: Used in developing new active ingredients for crop protection products, leveraging its heterocyclic core structure.
• Organic Synthesis Reagent: Serves as a precursor or reactant in complex multi-step organic syntheses for academic and industrial research.
• Biochemical Tool Compound: Utilized in life science research to study enzyme interactions or receptor binding mechanisms related to barbiturate activity.
• Material Science Research: Investigated as a potential component in the development of specialty polymers or organic electronic materials.

Basic Information

Product Name	5-(2-Methoxybenzylidene)-1,3-Dimethylpyrimidine-2,4,6(1H,3H,5H)-Trione
CAS No.	57270-83-4
Molecular Formula	C14H14N2O4
Molecular Weight	274.27 g/mol
Synonyms	5-(2-Methoxybenzylidene)-1,3-dimethylbarbituric acid; 1,3-Dimethyl-5-(2-methoxybenzylidene)barbituric acid; 5-(2-Methoxybenzylidene)-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione; 2-Methoxybenzylidene Meldrum's acid derivative (related analog); 5-(o-Methoxybenzylidene)-1,3-dimethylbarbituric acid
EINECS	Contact for details

Quality Control

Our 5-(2-Methoxybenzylidene)-1,3-Dimethylpyrimidine-2,4,6(1H,3H,5H)-Trione is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods (NMR, IR), to ensure it meets the high standards required for research and development applications. Certificates of Analysis (COA) detailing batch-specific results are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials such as strong oxidizing agents.

Specification

Item	Specification
Appearance	Off-white to pale yellow crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Melting Point	Contact for details
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.