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Home  > 2-((tert-Butoxycarbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid

AU76874

1219406-23-1 | 2-((tert-Butoxycarbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $806.00 $565.00 -   +
1g 95% in stock $2,547.00 $1,783.00 -   +
5g 95% in stock $7,629.00 $5,341.00 -   +
10g 95% in stock $10,676.00 $7,473.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AU76874
Chemical Name: 2-((tert-Butoxycarbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid
CAS Number: 1219406-23-1
Molecular Formula: C18H32N2O6
Molecular Weight: 372.4565
MDL Number: MFCD10687137
SMILES: O=C(OC(C)(C)C)NC(C(=O)O)CC1CCN(CC1)C(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • 2-((tert-butoxycarbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid, also known as $name$, is a versatile compound commonly employed in chemical synthesis as a protecting group for amino acids. This molecule serves as a crucial tool in organic chemistry, allowing for the selective protection of amine functionalities during various synthetic processes.The tert-butoxycarbonyl (Boc) protecting group attached to the amino group of the molecule imparts steric hindrance, shielding the amine from unwanted reactions while the synthesis proceeds. This protection enables chemists to manipulate other parts of the molecule without affecting the amine functionality, providing control over the sequence of reactions and ensuring the desired outcome.Moreover, the presence of the piperidine ring in the structure of $name$ offers additional flexibility in the design of peptide and drug molecules. The piperidine moiety can participate in various interactions, influencing the pharmacological properties of the final products synthesized using this compound.Overall, the strategic incorporation of 2-((tert-butoxycarbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid in chemical synthesis empowers chemists to carry out complex reactions with precision and control, paving the way for the creation of novel compounds with diverse applications in pharmaceuticals, materials science, and biotechnology.
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