7531-52-4 | L-Prolinamide

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$6.00	$4.00
10g	97%	in stock	$8.00	$5.00
25g	97%	in stock	$13.00	$9.00
500g	97%	in stock	$109.00	$76.00

Description

• Catalog Number: AB46254
• Chemical Name: L-Prolinamide
• CAS Number: 7531-52-4
• Molecular Formula: C5H10N2O
• Molecular Weight: 114.1457
• MDL Number: MFCD00005253
• SMILES: NC(=O)[C@@H]1CCCN1

Computed Properties

• Complexity: 103
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: -0.9

Upstream Synthesis Route

L-Prolinamide, also known as proline amide, plays a crucial role in chemical synthesis as a versatile building block and reagent. Its unique structure and properties make it valuable in various synthetic processes, particularly in the field of organic chemistry.One key application of L-Prolinamide is its use as a chiral auxiliary in asymmetric synthesis. Due to the chirality of proline, L-Prolinamide can help induce asymmetry in reactions, enabling the synthesis of enantiomerically pure compounds. This is especially useful in the production of pharmaceuticals, agrochemicals, and other fine chemicals where enantiomeric purity is essential for biological activity or desired properties.Additionally, L-Prolinamide can act as a highly efficient catalyst in a variety of organic transformations such as aldol reactions, Michael additions, and asymmetric hydrogenations. Its ability to activate substrates and control stereoselectivity makes it a valuable tool for chemists seeking to produce complex molecules with high levels of chiral purity.In conclusion, the versatility and unique properties of L-Prolinamide make it a valuable tool in chemical synthesis, particularly in the preparation of chiral compounds and complex organic molecules. By harnessing its reactivity and selectivity, chemists can access a wide range of synthetic pathways and achieve efficient and selective transformations in their research and development endeavors.