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72072-06-1

N-Boc-5-aminolevulinic acid

Catalog#: AR00FD2C  |   CAS#: 72072-06-1  |   MDL#: MFCD02682635  |   MF: C10H17NO5  |   MW: 231.2457

Packsize Purity Price Availability Quantity
100mg 95% $27.00 Global Stock Buy Now Add To Cart
250mg 95% $60.00 Global Stock Buy Now Add To Cart
1g 95% $173.00 Global Stock Buy Now Add To Cart
5g 95% $799.00 Global Stock Buy Now Add To Cart
10g 95% $1,376.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00FD2C
Chemical Name N-Boc-5-aminolevulinic acid
CAS Number 72072-06-1
Molecular Formula C10H17NO5
Molecular Weight 231.2457
MDL Number MFCD02682635
SMILES O=C(CNC(=O)OC(C)(C)C)CCC(=O)O

5-((tert-Butoxycarbonyl)amino)-4-oxopentanoic acid, commonly known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a crucial building block in peptide and pharmaceutical synthesis due to its unique structural properties and reactivity.$name$ is particularly valuable in peptide synthesis, where it acts as a key intermediate in the formation of peptide bonds. Its tert-butoxycarbonyl (Boc) protecting group plays a vital role in safeguarding specific functional groups during various synthetic steps, allowing for precise manipulation and control of chemical reactions. Additionally, the presence of the oxo (keto) group on the pentanoic acid moiety provides opportunities for further derivatization and modification, enhancing the versatility of $name$ in designing complex peptide structures.Furthermore, $name$ finds extensive applications in the pharmaceutical industry for the synthesis of novel drug candidates and bioactive molecules. Its strategic placement within the chemical scaffold of pharmaceutical compounds imparts unique pharmacological properties, making it a valuable tool for drug discovery and development. By incorporating $name$ into synthetic pathways, chemists can access diverse chemical space, enabling the creation of structurally diverse and biologically active compounds.In summary, the strategic incorporation of 5-((tert-Butoxycarbonyl)amino)-4-oxopentanoic acid in chemical synthesis empowers researchers to design and construct intricate peptide sequences and pharmaceutical compounds with precision and efficiency. Its pivotal role in maintaining chemical stability and enabling selective reactions makes it an indispensable component in the toolkit of synthetic chemists and pharmaceutical scientists alike.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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