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115655-41-9

4-AMINO-1-CBZ-PIPERIDINE-4-CARBOXYLIC ACID

Catalog#: AR000HED  |   CAS#: 115655-41-9  |   MDL#: MFCD03425218  |   MF: C14H18N2O4  |   MW: 278.3037

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Catalog Number AR000HED
Chemical Name 4-AMINO-1-CBZ-PIPERIDINE-4-CARBOXYLIC ACID
CAS Number 115655-41-9
Molecular Formula C14H18N2O4
Molecular Weight 278.3037
MDL Number MFCD03425218
SMILES O=C(N1CCC(CC1)(N)C(=O)O)OCc1ccccc1

4-Amino-1-cbz-piperidine-4-carboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various synthetic processes due to its unique structural properties and reactivities.In organic chemistry, $name$ is commonly employed as a key building block for the synthesis of complex molecules. Its amino and carboxylic acid functional groups make it a valuable intermediate for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of a piperidine ring in $name$ confers steric and electronic properties that are favorable for diverse synthetic transformations.One of the primary applications of 4-Amino-1-cbz-piperidine-4-carboxylic acid in chemical synthesis is in peptide chemistry. Peptides, which are short chains of amino acids linked by peptide bonds, are essential biomolecules with various biological activities. $name$ can be utilized as a protected amino acid derivative in peptide synthesis, where it serves as a building block for the assembly of peptide chains. By selectively deprotecting the carbobenzyloxy (Cbz) group in $name$, specific amino acids can be incorporated into peptide sequences with high purity and efficiency.Additionally, the functional groups present in 4-Amino-1-cbz-piperidine-4-carboxylic acid enable its use in the development of new materials, catalysts, and bioconjugates. Through rational design and modification, this compound can be tailored to exhibit desired properties for a wide range of applications in the fields of chemistry and materials science.Overall, the versatile nature of $name$ makes it a valuable reagent in synthetic chemistry, offering a platform for the creation of diverse molecular structures with potential applications in pharmaceuticals, materials, and beyond.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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