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518048-05-0

N-[2-[4-[(4-fluorophenyl)methylcarbamoyl]-5-hydroxy-1-methyl-6-oxopyrimidin-2-yl]propan-2-yl]-5-methyl-1,3,4-oxadiazole-2-carboxamide

Catalog#: AR00I9YM  |   CAS#: 518048-05-0  |   MDL#: MFCD10698872  |   MF: C20H21FN6O5  |   MW: 444.4163

Packsize Purity Price Availability Quantity
5mg 97% $5.00 Global Stock Buy Now Add To Cart
10mg 97% $8.00 Global Stock Buy Now Add To Cart
50mg 97% $20.00 Global Stock Buy Now Add To Cart
100mg 97% $24.00 Global Stock Buy Now Add To Cart
250mg 97% $48.00 Global Stock Buy Now Add To Cart
1g 97% $128.00 Global Stock Buy Now Add To Cart
5g 97% $439.00 Global Stock Buy Now Add To Cart
25g 97% $2,147.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00I9YM
Chemical Name N-[2-[4-[(4-fluorophenyl)methylcarbamoyl]-5-hydroxy-1-methyl-6-oxopyrimidin-2-yl]propan-2-yl]-5-methyl-1,3,4-oxadiazole-2-carboxamide
CAS Number 518048-05-0
Molecular Formula C20H21FN6O5
Molecular Weight 444.4163
MDL Number MFCD10698872
SMILES Fc1ccc(cc1)CNC(=O)c1nc(n(c(=O)c1O)C)C(NC(=O)c1nnc(o1)C)(C)C

N-(2-(4-((4-Fluorobenzyl)carbamoyl)-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide, commonly known as $name$, is a versatile compound with significant utility in chemical synthesis processes. In the realm of organic chemistry, $name$ serves as a crucial intermediate in the creation of complex molecules and pharmaceuticals. Its unique structure and functional groups make it a valuable building block for the synthesis of various biologically active compounds.The presence of the oxadiazole ring in $name$ confers enhanced reactivity and specificity, allowing for precise control over chemical reactions. This compound plays a key role in the construction of heterocyclic compounds, which are prevalent in medicinal chemistry and drug development. By incorporating $name$ into synthetic pathways, chemists can access diverse chemical space and generate novel compounds with potential therapeutic applications.Moreover, the presence of the hydroxy and carbamoyl groups in $name$ enables the introduction of additional functionalities during chemical transformations. These reactive moieties facilitate the attachment of different substituents, thereby modulating the physicochemical properties and biological activities of the final products. Through strategic manipulation of $name$ in synthesis, chemists can tailor molecular structures to achieve specific properties desired for various applications.Overall, the strategic incorporation of N-(2-(4-((4-Fluorobenzyl)carbamoyl)-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide, or $name$, in chemical synthesis processes opens up opportunities for the construction of diverse chemical scaffolds and the development of new compounds with promising biological activities.
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