Pentanoic acid,2-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]-4-methyl-, (2S)-


Chemical Name: Pentanoic acid,2-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]-4-methyl-, (2S)-
CAS Number: 828254-18-8
Product Number: AG00G839(AGN-PC-0UNAP1)
Synonyms:
MDL No:
Molecular Formula: C12H23NO4
Molecular Weight: 245.3153

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(S)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in organic chemistry due to its ability to serve as a key building block in the creation of various pharmaceuticals, fine chemicals, and advanced materials.One significant application of (S)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid in chemical synthesis is its use as a chiral auxiliary. In asymmetric synthesis, this compound can act as a valuable tool for introducing chirality into organic molecules. By utilizing (S)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid as a chiral template, chemists can selectively create enantiomerically pure compounds, which is essential in the development of pharmaceuticals and other high-value products.Furthermore, (S)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid is employed in the synthesis of peptide-based molecules. As a protected amino acid derivative, this compound can be utilized in peptide chemistry to introduce specific functionalities at desired positions in the peptide chain. By incorporating (S)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid into peptide synthesis, chemists can achieve precise control over the structure and properties of the resulting peptides, enabling the creation of novel bioactive compounds and biomaterials.In summary, the versatile nature of (S)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid makes it an indispensable tool in chemical synthesis, particularly in the development of chiral compounds and peptide-based materials. Its applications in asymmetric synthesis and peptide chemistry highlight its significance in advancing the field of organic chemistry and enabling the creation of complex and valuable molecules with tailored properties.