116247-92-8 | 1-Pyrimidin-2-yl-piperidin-4-one

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$40.00	$28.00
5g	97%	in stock	$169.00	$118.00
10g	97%	in stock	$249.00	$175.00
25g	97%	in stock	$510.00	$357.00
100g	97%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AA15397
• Chemical Name: 1-Pyrimidin-2-yl-piperidin-4-one
• CAS Number: 116247-92-8
• Molecular Formula: C9H11N3O
• Molecular Weight: 177.2031
• MDL Number: MFCD00231572
• SMILES: O=C1CCN(CC1)c1ncccn1

Computed Properties

• Complexity: 179
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• XLogP3: 0.1

Upstream Synthesis Route

1-Pyrimidin-2-yl-piperidin-4-one, also known as $name$, is a versatile compound commonly used in chemical synthesis as a key building block for the preparation of various biologically active molecules. Due to its unique structural features, $name$ serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 1-Pyrimidin-2-yl-piperidin-4-one can be used as a starting material for the preparation of heterocyclic compounds with diverse functional groups. Its reactive nature allows for facile derivatization, making it a valuable tool for the modification of molecular structures to fine-tune desired properties. Additionally, the presence of the pyrimidine and piperidine moieties in $name$ enhances the biological activity and pharmacokinetic profile of the final products.Moreover, the strategic placement of functional groups in 1-Pyrimidin-2-yl-piperidin-4-one enables chemists to introduce chirality and stereochemistry into their target molecules, making it a useful chiral auxiliary in asymmetric synthesis. By incorporating $name$ into synthetic pathways, researchers can access a wide range of enantiomerically pure compounds with high selectivity and efficiency.Overall, the application of 1-Pyrimidin-2-yl-piperidin-4-one in chemical synthesis offers exciting possibilities for the development of novel compounds with enhanced biological activity and structural diversity. Its utility as a versatile building block underscores its importance in modern synthetic chemistry and drug discovery efforts.