116041-19-1 | 1-Benzyl-5-oxo-3-pyrrolidinecarboxamide

Packsize	Purity	Availability	Price	Discounted Price
250mg	94%	in stock	$20.00	$14.00
1g	94%	in stock	$49.00	$34.00
5g	94%	in stock	$153.00	$107.00
10g	94%	in stock	$265.00	$186.00
25g	94%	in stock	$510.00	$357.00
100g	94%	in stock	$1,317.00	$922.00

Description

• Catalog Number: AA14626
• Chemical Name: 1-Benzyl-5-oxo-3-pyrrolidinecarboxamide
• CAS Number: 116041-19-1
• Molecular Formula: C12H14N2O2
• Molecular Weight: 218.25176000000008
• MDL Number: MFCD00173111
• SMILES: NC(=O)C1CN(C(=O)C1)Cc1ccccc1

Computed Properties

• Complexity: 285
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: -0.2

Upstream Synthesis Route

1-Benzyl-5-oxopyrrolidine-3-carboxamide, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and functionalities. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. With its structural framework, $name$ exhibits excellent reactivity and selectivity, making it an essential intermediate in the synthesis of complex organic molecules.In chemical synthesis, $name$ is commonly employed as a nucleophilic amide that can undergo a range of transformations to introduce diverse functional groups into a target molecule. Its reactivity at the amide carbonyl group enables efficient derivatization through amidation, transamidation, and amidocarbonylation reactions. Additionally, the benzyl group attached to the pyrrolidine ring provides stability and protection to the amide functionality, allowing for selective modifications at other sites within the molecule.Moreover, the presence of the oxo group in $name$ offers opportunities for further functionalization through various reduction or oxidation reactions, expanding its synthetic utility in the creation of structurally diverse compounds. Overall, the strategic incorporation of 1-Benzyl-5-oxopyrrolidine-3-carboxamide in chemical synthesis enables chemists to access novel molecular scaffolds and access valuable intermediates with high efficiency and precision.