270062-83-4 | Fmoc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	99%	in stock	$20.00	$14.00
250mg	99%	in stock	$26.00	$18.00
1g	99%	in stock	$96.00	$67.00
10g	95%	in stock	$946.00	$662.00
25g	95%	in stock	$1,879.00	$1,316.00

Description

• Catalog Number: AB51233
• Chemical Name: Fmoc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid
• CAS Number: 270062-83-4
• Molecular Formula: C25H22FNO4
• Molecular Weight: 419.4449
• MDL Number: MFCD01861013
• SMILES: OC(=O)C[C@H](Cc1ccc(cc1)F)NC(=O)OCC1c2ccccc2c2c1cccc2

Computed Properties

• Complexity: 599
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 31
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 8
• XLogP3: 4.7

Upstream Synthesis Route

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-fluorophenyl)butanoic acid, commonly known as $name$, is a highly versatile compound that plays a crucial role in chemical synthesis. This compound is widely utilized as a chiral building block in the creation of complex molecules due to its unique stereochemical properties. In organic synthesis, $name$ serves as a pivotal component for the development of pharmaceuticals, agrochemicals, and advanced materials. Its chirality allows for the precise control of molecular structure, enabling chemists to design and produce compounds with specific biological activities and desirable properties. Incorporating $name$ into synthesis pathways provides a powerful tool for achieving enantiopure products, essential in drug discovery and development. Furthermore, its ability to act as a key intermediate in the formation of diverse chemical entities underscores its significance as a valuable reagent in the realm of modern synthetic chemistry.