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AA21046

115186-37-3 | N-(tert-Butoxycarbonyl)-l-proline n'-methoxy-n'-methylamide

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $49.00 $34.00 -   +
5g 97% in stock $155.00 $108.00 -   +
25g 97% in stock $573.00 $402.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA21046
Chemical Name: N-(tert-Butoxycarbonyl)-l-proline n'-methoxy-n'-methylamide
CAS Number: 115186-37-3
Molecular Formula: C12H22N2O4
Molecular Weight: 258.3141
MDL Number: MFCD00209555
SMILES: COCNC(=O)[C@@H]1CCCN1C(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • Boc-Pro-NMe(OMe) is a versatile chemical compound widely used in organic synthesis. This compound serves as a valuable building block for the construction of complex molecules in the field of medicinal chemistry, pharmaceuticals, and materials science. Its unique structural properties make it particularly useful in peptide synthesis and modification.In chemical synthesis, Boc-Pro-NMe(OMe) can act as a protected amino acid derivative, providing a means to introduce specific functional groups at precise positions within a molecule. The Boc (tert-butyloxycarbonyl) group serves as a protective unit for the amino group, allowing chemists to selectively manipulate other parts of the molecule without affecting the desired amino acid functionality. This selective protection-deprotection strategy is crucial for the controlled assembly of peptides and small organic molecules.Furthermore, the N-methyl and O-methyl functionalities in Boc-Pro-NMe(OMe) offer additional flexibility in synthetic routes by enabling further derivatization and enhancing the compound's solubility and stability. These features make Boc-Pro-NMe(OMe) a valuable tool in the design and synthesis of bioactive compounds, peptidomimetics, and other structurally diverse molecules with tailored properties.Overall, Boc-Pro-NMe(OMe) plays a key role in enabling chemists to perform intricate manipulations and achieve specific chemical transformations, making it an indispensable component in various synthetic methodologies.
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