Description
Methyl 2-(4-benzamido-2-oxopyrimidin-1(2H)-yl)acetate (CAS No. 172405-13-9) is a high-purity synthetic organic compound with the molecular formula C14H13N3O4. This specialized chemical features a pyrimidinone core functionalized with a benzamido group at the 4-position and an ester-linked methyl acetate moiety at the 1-position. The compound’s unique structure makes it valuable for pharmaceutical research, particularly in the development of nucleoside analogs and enzyme inhibitors. Offered as a white to off-white crystalline powder, our product is rigorously tested to ensure ≥95% purity by HPLC analysis. Suitable for medicinal chemistry applications, this building block is provided in sealed packaging under inert atmosphere to guarantee stability. Researchers can request custom quantities from milligram to kilogram scale with optional analytical documentation including 1H NMR, 13C NMR, and mass spectrometry data.
Properties
- CAS Number: 172405-13-9
- Complexity: 492
- IUPAC Name: methyl 2-(4-benzamido-2-oxo-pyrimidin-1-yl)acetate
- InChI: InChI=1S/C14H13N3O4/c1-21-12(18)9-17-8-7-11(16-14(17)20)15-13(19)10-5-3-2-4-6-10/h2-8H,9H2,1H3,(H,15,16,19,20)
- InChI Key: UTOUVTVKVWBZMU-UHFFFAOYSA-N
- Exact Mass: 287.09060590
- Molecular Formula: C14H13N3O4
- Molecular Weight: 287.27
- SMILES: COC(=O)CN1C=CC(=NC1=O)NC(=O)C2=CC=CC=C2
- Topological: 88.1
- Monoisotopic Mass: 287.09060590
- Synonyms: Methyl 2-(4-benzamido-2-oxopyrimidin-1(2H)-yl)acetate, 172405-13-9
Application
This compound serves as a key intermediate in the synthesis of modified nucleosides with potential antiviral or anticancer activity. Researchers utilize it for developing pyrimidine-based protease inhibitors targeting viral replication enzymes. The benzamido and ester functionalities provide convenient handles for further structural modifications through amide coupling or hydrolysis reactions. In medicinal chemistry programs, it has shown promise as a scaffold for kinase inhibitor development.
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