L-Valine, 1-methylethyl ester, with the CAS number 61393-65-5, is an ester derivative of the amino acid L-valine. This compound features a branched-chain structure, characteristic of valine, which contributes to its hydrophobic properties. As an ester, it typically exhibits lower polarity compared to its parent amino acid, influencing its solubility in various organic solvents. L-Valine itself is essential for protein synthesis and plays a crucial role in muscle metabolism and tissue repair. The esterification process can enhance the compound's stability and bioavailability, making it of interest in pharmaceutical and nutritional applications. In terms of physical properties, L-Valine esters may have distinct melting and boiling points compared to the free amino acid, and their reactivity can be influenced by the ester functional group. Overall, L-Valine, 1-methylethyl ester is significant in biochemical research and potential therapeutic formulations, particularly in contexts where enhanced absorption or specific metabolic pathways are desired.

L-Valine, 1-methylethyl ester

61393-65-5: L-Valine, 1-methylethyl ester, with the CAS number 61393-65-5, is an ester derivative of the amino acid L-valine. This compound features a branched-chain structure, characteristic of valine, which contributes to its hydrophobic properties. As an ester, it typically exhibits lower polarity compared to its parent amino acid, influencing its solubility in various organic solvents. L-Valine itself is essential for protein synthesis and plays a crucial role in muscle metabolism and tissue repair. The esterification process can enhance the compound's stability and bioavailability, making it of interest in pharmaceutical and nutritional applications. In terms of physical properties, L-Valine esters may have distinct melting and boiling points compared to the free amino acid, and their reactivity can be influenced by the ester functional group. Overall, L-Valine, 1-methylethyl ester is significant in biochemical research and potential therapeutic formulations, particularly in contexts where enhanced absorption or specific metabolic pathways are desired.

<p>Propan-2-yl (2S)-2-amino-3-methylbutanoate is an amino acid derivative that is used as a chiral auxiliary. The compound has been used in the synthesis of amides, esters, and other amine products. It has also been used in the preparation of enantiomerically pure protonated amines. Propan-2-yl (2S)-2-amino-3-methylbutanoate can be used as a chiral auxiliary in chromatographic techniques to separate racemic mixtures into their enantiomers. This compound is mesomorphic at low temperatures and becomes isotropic at higher temperatures. Propan-2-yl (2S)-2-amino-3-methylbutanoate is also soluble in solvents with different polarities, such as water and chloroform, and has a molecular weight of 158.25 g/mol.</p>

CAS 61393-65-5

L-Valine, 1-methylethyl ester

Propan-2-yl (2S)-2-amino-3-methylbutanoate

Ref: 3D-LCA39365