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Home  > (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid

AA54079

1217662-55-9 | (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $81.00 $57.00 -   +
250mg 95% in stock $142.00 $100.00 -   +
1g 95% in stock $377.00 $264.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA54079
Chemical Name: (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid
CAS Number: 1217662-55-9
Molecular Formula: C22H19NO5
Molecular Weight: 377.38996
MDL Number: MFCD04117844
SMILES: O=C(N[C@@H](c1ccco1)CC(=O)O)OCC1c2ccccc2-c2c1cccc2

 

Upstream Synthesis Route
  • The application of (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid in chemical synthesis lies in its crucial role as a chiral building block. This compound, often referred to as a chiral amino acid derivative, can serve as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials.Specifically, the (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid can be utilized in the asymmetric synthesis of biologically active molecules due to its unique stereochemistry. Its chiral nature allows for the creation of enantiopure compounds, enabling researchers to access specific enantiomers with high optical purity, which is essential for many applications in the pharmaceutical industry.Furthermore, this compound can participate in different chemical reactions such as amide bond formation, enzymatic transformations, and peptide coupling reactions. Its versatility in forming diverse chemical bonds makes it a valuable tool in the development of complex molecules with precise stereochemical control.Overall, the (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid plays a critical role in modern organic synthesis, offering chemists a powerful means to access chiral compounds necessary for cutting-edge research and drug discovery efforts.
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