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Product Line: Pharmaceutical Chemicals

4-Boc-2-morpholinecarboxylic acid

CAS 189321-66-2

Molecular structure of 4-Boc-2-morpholinecarboxylic acid

CAS · 189321-66-2

01

Product Overview

4-Boc-2-morpholinecarboxylic acid is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance: Off-white or light brown solid
Purity: 97% min
Water: 0.5% max
03

Applications

4-Boc-2-morpholinecarboxylic acid (CAS 189321-66-2) is a protected amino acid derivative widely used in organic synthesis and pharmaceutical research. The Boc (tert-butoxycarbonyl) protecting group safeguards the amino functionality, allowing selective reactions on the carboxyl group or morpholine ring. It serves as a key intermediate for the synthesis of peptides, heterocyclic compounds, and bioactive molecules. In medicinal chemistry, it is applied to develop CNS-active agents, enzyme inhibitors, and other therapeutic compounds. Its protected structure also facilitates stepwise synthesis in drug discovery, enabling chemists to construct complex molecules with high efficiency and minimal side reactions.

04

Benefits

The benefits of 4-Boc-2-morpholinecarboxylic acid stem from its stability, protection strategy, and versatility in chemical reactions. The Boc group provides temporary protection of the amino group, preventing unwanted side reactions during multi-step synthesis. Its carboxyl group and morpholine moiety offer reactive sites for amide bond formation, cyclization, or substitution reactions, enabling the creation of diverse derivatives. The compound's stability under standard laboratory conditions makes it easy to store and handle, while its reactivity ensures efficient incorporation into peptides, heterocycles, and pharmaceutical intermediates.

05

Conclusion

4-Boc-2-morpholinecarboxylic acid is a versatile and stable intermediate used in peptide synthesis, medicinal chemistry, and heterocyclic compound development. Its Boc protection strategy, combined with reactive carboxyl and morpholine functionalities, allows efficient construction of complex bioactive molecules. By providing selectivity, stability, and synthetic flexibility, it remains an important tool in drug discovery and chemical research.

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