1251904-51-4 | (S)-N-Fmoc-2-(5'-pentenyl)glycine

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$51.00	$36.00
250mg	97%	in stock	$80.00	$56.00
1g	97%	in stock	$237.00	$166.00
5g	97%	in stock	$953.00	$667.00

Description

• Catalog Number: AA30040
• Chemical Name: (S)-N-Fmoc-2-(5'-pentenyl)glycine
• CAS Number: 1251904-51-4
• Molecular Formula: C23H25NO4
• Molecular Weight: 379.4489
• MDL Number: MFCD03094929
• SMILES: C=CCCCC[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2-c2c1cccc2

Computed Properties

• Complexity: 527
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 28
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 10
• XLogP3: 5

Upstream Synthesis Route

The (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)oct-7-enoic acid, which will be referred to as $name$, is a highly versatile compound frequently utilized in chemical synthesis. Its unique molecular structure and reactivity make it an indispensable tool for synthetic chemists across various industries.One key application of $name$ in chemical synthesis is as a chiral building block for the asymmetric synthesis of complex molecules. Due to the presence of a chiral center in its structure, $name$ can impart chirality to target compounds, enabling the production of enantiomerically pure substances. This is particularly valuable in the pharmaceutical industry, where the stereochemistry of a molecule can significantly impact its biological activity and pharmacological properties.Furthermore, the presence of functional groups in $name$, such as the carbamate and carboxylic acid moieties, allows for a range of chemical transformations, including amidation, esterification, and peptide coupling reactions. These versatile functional groups enable the incorporation of $name$ into diverse molecular frameworks, enhancing the synthetic flexibility and efficiency of chemical processes.In summary, (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)oct-7-enoic acid, $name$, serves as a valuable building block in chemical synthesis, facilitating the construction of complex and chiral molecules with broad applications in pharmaceuticals, agrochemicals, and materials science.