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768371-16-0

Ethyl 4-Boc-2-morpholinecarboxylate

Catalog#: AR003QYU  |   CAS#: 768371-16-0  |   MDL#: MFCD01646390  |   MF: C12H21NO5  |   MW: 259.29884000000004

Packsize Purity Price Availability Quantity
250mg 95% $4.00 Global Stock Buy Now Add To Cart
1g 95% $5.00 Global Stock Buy Now Add To Cart
5g 95% $21.00 Global Stock Buy Now Add To Cart
10g 95% $42.00 Global Stock Buy Now Add To Cart
25g 95% $96.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003QYU
Chemical Name Ethyl 4-Boc-2-morpholinecarboxylate
CAS Number 768371-16-0
Molecular Formula C12H21NO5
Molecular Weight 259.29884000000004
MDL Number MFCD01646390
SMILES CCOC(=O)C1OCCN(C1)C(=O)OC(C)(C)C

Ethyl 4-Boc-2-morpholinecarboxylate, also known by its systematic name ethyl 2-(2-morpholino)-2-oxoethyl carbamate, is a versatile compound that finds a wide range of applications in chemical synthesis. This compound serves as a valuable building block in organic synthesis due to its unique structure and reactivity.One of the key applications of Ethyl 4-Boc-2-morpholinecarboxylate is its use as a protecting group in peptide synthesis. The Boc (tert-butoxycarbonyl) group is commonly employed to temporarily protect the amine group of amino acids during peptide assembly. By selectively installing and removing the Boc group as needed, chemists can control the sequence of amino acids in the final peptide product. This strategy enables the synthesis of complex peptides and peptidomimetics with high efficiency and precision.Additionally, Ethyl 4-Boc-2-morpholinecarboxylate can be utilized as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and functional materials. Its versatile reactivity allows for the introduction of diverse functional groups and structural motifs, enabling the rapid construction of molecular scaffolds with desired properties.Overall, Ethyl 4-Boc-2-morpholinecarboxylate plays a crucial role in modern organic synthesis as a valuable tool for building complex molecules with specific functionalities. Its applications in peptide chemistry and drug discovery highlight its importance in advancing the field of chemical synthesis.
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