110990-07-3 | Fmoc-D-Lys(Z)-OH

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$16.00	$11.00
1g	97%	in stock	$22.00	$15.00
5g	97%	in stock	$45.00	$31.00
25g	97%	in stock	$153.00	$107.00
100g	97%	in stock	$510.00	$357.00

Description

• Catalog Number: AD41562
• Chemical Name: Fmoc-D-Lys(Z)-OH
• CAS Number: 110990-07-3
• Molecular Formula: C29H30N2O6
• Molecular Weight: 502.5583
• MDL Number: MFCD00065663
• SMILES: O=C(OCc1ccccc1)NCCCC[C@H](C(=O)O)NC(=O)OCC1c2ccccc2-c2c1cccc2

Upstream Synthesis Route

The chemical compound (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((benzyloxy)carbonyl)amino)hexanoic acid, also known as $name$, is a versatile tool in chemical synthesis. Its unique structure allows for precise manipulation and modification of molecules in a controlled manner. One of the key applications of $name$ in chemical synthesis is as a chiral building block. The chiral nature of this compound, with the (R) configuration, makes it a valuable starting material for asymmetric synthesis. By incorporating (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((benzyloxy)carbonyl)amino)hexanoic acid into a synthetic pathway, chemists can introduce chirality into their target molecules with high selectivity and efficiency.Furthermore, $name$ can serve as a protecting group for amines and carboxylic acids. The fluorenyl and benzyloxycarbonyl functionalities provide temporary shielding for reactive functional groups during chemical reactions, preventing unwanted side reactions and ensuring the desired transformations occur smoothly.In summary, the strategic incorporation of (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((benzyloxy)carbonyl)amino)hexanoic acid in chemical synthesis enables precise control over stereochemistry, as well as protection of key functional groups, making it a valuable asset for synthetic chemists seeking to design and construct complex molecules.