The chemical substance known as L-Valine, N-(2-chloroacetyl)-, 1,1-dimethylethyl ester is a derivative of the amino acid valine, which is essential for protein synthesis and plays a crucial role in various metabolic processes. This compound features a chloroacetyl group, which can enhance its reactivity and potential biological activity. The presence of the 1,1-dimethylethyl ester moiety suggests that it may exhibit lipophilic properties, potentially influencing its solubility and permeability in biological systems. The CAS number 1909295-01-7 uniquely identifies this compound, facilitating its recognition in chemical databases and literature. As a synthetic derivative, it may be explored for applications in pharmaceuticals, particularly in drug design or as a biochemical probe. The specific characteristics, such as melting point, boiling point, and spectral data, would require empirical measurement or literature reference for detailed analysis. Overall, this compound represents an interesting intersection of amino acid chemistry and synthetic organic chemistry, with potential implications in medicinal chemistry.

<span class="text-smallcaps">L</span>-Valine, N-(2-chloroacetyl)-, 1,1-dimethylethyl ester

1909295-01-7: The chemical substance known as L-Valine, N-(2-chloroacetyl)-, 1,1-dimethylethyl ester is a derivative of the amino acid valine, which is essential for protein synthesis and plays a crucial role in various metabolic processes. This compound features a chloroacetyl group, which can enhance its reactivity and potential biological activity. The presence of the 1,1-dimethylethyl ester moiety suggests that it may exhibit lipophilic properties, potentially influencing its solubility and permeability in biological systems. The CAS number 1909295-01-7 uniquely identifies this compound, facilitating its recognition in chemical databases and literature. As a synthetic derivative, it may be explored for applications in pharmaceuticals, particularly in drug design or as a biochemical probe. The specific characteristics, such as melting point, boiling point, and spectral data, would require empirical measurement or literature reference for detailed analysis. Overall, this compound represents an interesting intersection of amino acid chemistry and synthetic organic chemistry, with potential implications in medicinal chemistry.

CAS 1909295-01-7

<span class="text-smallcaps">L</span>-Valine, N-(2-chloroacetyl)-, 1,1-dimethylethyl ester

tert-Butyl (2S)-2-(2-chloroacetamido)-3-methylbutanoate

Ref: 3D-JBD29501