1050443-69-0 | (2R)-3-([(tert-Butoxy)carbonyl]amino)-2-(1h-indol-3-ylmethyl)propanoic acid

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Description

• Catalog Number: AE09124
• Chemical Name: (2R)-3-([(tert-Butoxy)carbonyl]amino)-2-(1h-indol-3-ylmethyl)propanoic acid
• CAS Number: 1050443-69-0
• Molecular Formula: C17H22N2O4
• Molecular Weight: 318.3676
• MDL Number: MFCD07372871
• SMILES: O=C(OC(C)(C)C)NC[C@H](C(=O)O)Cc1c[nH]c2c1cccc2

Upstream Synthesis Route

The compound (R)-2-((1H-indol-3-yl)methyl)-3-((tert-butoxycarbonyl)amino)propanoic acid, known for its chirality and unique structural properties, plays a crucial role in chemical synthesis as a versatile intermediate. This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly in the creation of peptidomimetics and diversified small molecules. Its strategic placement within synthetic pathways enables the introduction of the indole moiety and tert-butoxycarbonyl-protected amino group into the target molecules, facilitating the development of novel drug candidates and bioactive compounds. Additionally, the stereochemical purity of the (R) configuration is essential for maintaining the desired biological activity of the synthesized products. By harnessing the reactivity and selectivity of (R)-2-((1H-indol-3-yl)methyl)-3-((tert-butoxycarbonyl)amino)propanoic acid, chemists can efficiently access a wide range of molecular frameworks with tailored functionalities and enhanced pharmacological properties.