1217833-77-6 | Fmoc-(2r,3s)-2-amino-3-hydroxy-4-methylpentanoic acid

Availability
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Description

• Catalog Number: AA54215
• Chemical Name: Fmoc-(2r,3s)-2-amino-3-hydroxy-4-methylpentanoic acid
• CAS Number: 1217833-77-6
• Molecular Formula: C21H23NO5
• Molecular Weight: 369.41101999999995
• MDL Number: MFCD02682583
• SMILES: O=C(N[C@H]([C@H](C(C)C)O)C(=O)O)OCC1c2ccccc2-c2c1cccc2

Upstream Synthesis Route

The compound (2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-4-methylpentanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a chiral building block. Its unique structure and stereochemistry make it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and functional materials. In organic synthesis, $name$ can be used as a key starting material for the construction of complex molecules with specific stereochemical configurations. Its hydroxy and amino functional groups provide versatility in forming bonds with other molecules, enabling the creation of diverse chemical structures. The fluorenyl moiety in $name$ serves as a stable protecting group, safeguarding the reactivity of the amino group during synthetic transformations. Overall, the strategic incorporation of (2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-4-methylpentanoic acid in chemical synthesis offers a powerful tool for designing and accessing structurally diverse compounds with precise stereochemical attributes.