119479-32-2 | 2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$23.00	$17.00
5g	97%	in stock	$111.00	$78.00

Description

• Catalog Number: AA24246
• Chemical Name: 2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid
• CAS Number: 119479-32-2
• Molecular Formula: C10H17NO4
• Molecular Weight: 215.2463
• MDL Number: MFCD02682445
• SMILES: C=CCC(C(=O)O)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 255
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.7

Upstream Synthesis Route

2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid, commonly known as Boc-aminopentenoic acid, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the preparation of various peptides and peptidomimetics. Its functional groups enable specific interactions with other molecules, making it crucial in designing and creating novel molecules with desired biological activities.In peptide synthesis, Boc-aminopentenoic acid acts as a protected amino acid derivative that can be incorporated into peptide chains using solid-phase or solution-phase methods. Its tert-butoxycarbonyl (Boc) protecting group shields the amino group from unwanted reactions during the synthesis process, allowing for selective deprotection at a later stage. This controlled deprotection step is essential for the stepwise assembly of complex peptides with high purity.Moreover, the presence of the pent-4-enoic acid moiety in Boc-aminopentenoic acid offers additional chemical versatility. This unsaturated side chain can participate in various chemical transformations, such as cross-coupling reactions, cycloadditions, and modifications to introduce specific functionalities into the peptide backbone. These modifications can influence the peptide's conformation, stability, and biological activity, making Boc-aminopentenoic acid a valuable tool in peptide engineering and drug discovery.Overall, Boc-aminopentenoic acid plays a crucial role in the rational design and synthesis of bioactive peptides, peptidomimetics, and other complex molecules with diverse applications in medicinal chemistry, structural biology, and materials science. Its unique properties and compatibility with standard peptide chemistry make it an indispensable reagent for researchers and chemists working in the field of organic synthesis.