1014018-79-1 | (R)-Fmoc-4-amino-5-tert-butoxy-pentanoic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$159.00	$112.00
250mg	98%	in stock	$287.00	$201.00
1g	98%	in stock	$704.00	$493.00
5g	98%	in stock	$2,935.00	$2,055.00

Description

• Catalog Number: AE10867
• Chemical Name: (R)-Fmoc-4-amino-5-tert-butoxy-pentanoic acid
• CAS Number: 1014018-79-1
• Molecular Formula: C24H29NO5
• Molecular Weight: 411.4908
• MDL Number: MFCD05663766
• SMILES: OC(=O)CC[C@@H](NC(=O)OCC1c2ccccc2-c2c1cccc2)COC(C)(C)C

Upstream Synthesis Route

The compound (R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)pentanoic acid, commonly referred to as $name$, is a versatile molecule widely used in chemical synthesis. Its unique structure and properties make it an essential tool in various organic reactions and transformations.In chemical synthesis, $name$ serves as a key building block for creating complex molecules due to its ability to participate in multiple reactions. It is particularly valuable in peptide synthesis, where the amino acid moiety can be modified to introduce specific functionalities or stereochemistry. The fluorenyl group provides stability and protection to the amino acid, allowing for controlled reactions and precise manipulation of the molecule.Additionally, the tert-butoxy group plays a crucial role in enhancing the solubility and reactivity of the compound, making it easier to handle and optimize in different synthetic pathways. By strategically incorporating $name$ into a synthesis route, chemists can access novel compounds and streamline the production of pharmaceuticals, agrochemicals, and materials with tailored properties.Overall, the application of (R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)pentanoic acid in chemical synthesis opens up a world of possibilities for designing and constructing complex molecules with precision and efficiency.