118-78-5 | 5-Aminopyrimidine-2,4,6(1H,3H,5H)-trione

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$272.00	$190.00
5g	95%	in stock	$549.00	$384.00

Description

• Catalog Number: AB80303
• Chemical Name: 5-Aminopyrimidine-2,4,6(1H,3H,5H)-trione
• CAS Number: 118-78-5
• Molecular Formula: C4H5N3O3
• Molecular Weight: 143.1008
• MDL Number: MFCD00023873
• SMILES: NC1C(=O)NC(=O)NC1=O

Upstream Synthesis Route

5-Aminopyrimidine-2,4,6(1H,3H,5H)-trione is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. In organic chemistry, it serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its inherent ability to participate in diverse chemical reactions makes it a valuable building block for the preparation of complex molecules.One of the primary applications of 5-Aminopyrimidine-2,4,6(1H,3H,5H)-trione is in the synthesis of heterocyclic compounds, which are essential structural motifs found in many bioactive molecules. By reacting with different reagents and catalysts, this compound can undergo various transformations such as cyclization, acylation, and alkylation to generate novel heterocycles with specific pharmacological or biological properties. Additionally, its nitrogen-rich scaffold lends itself well to the incorporation of functional groups that can further enhance the desired reactivity and properties of the target molecules.Furthermore, 5-Aminopyrimidine-2,4,6(1H,3H,5H)-trione is utilized in the development of ligands for metal-catalyzed reactions, where its nitrogen atoms can coordinate with transition metals to facilitate catalytic processes. This compound also finds application in the preparation of chiral catalysts and organocatalysts, enabling the stereoselective synthesis of enantiopure compounds.Overall, the versatility and reactivity of 5-Aminopyrimidine-2,4,6(1H,3H,5H)-trione make it an indispensable tool in the toolbox of synthetic chemists for the efficient and selective construction of complex organic molecules with diverse applications in the fields of medicinal chemistry, materials science, and agrochemical research.