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Product Name: | Nval-Otbu.Hcl | CAS No: | 119483-47-5 |
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M.W: | 209.71 | MF: | C9H20ClNO2 |
Appearance: | White Powder | Purity: | 98+ |
EINECS No: | - | Storage: | 5-25°C |
Product Description
White Powder Nval-Otbu.Hcl CAS NO. 119483-47-5 Purity 98+
Name: Nval-Otbu.Hcl
CAS NO: 119483-47-5
M.W: 209.71
Appearance: White Powder
Purity: 98+
Synonyms: l-norvaline1,1-dimethylethylesterhydrochloride;L-NORVALINET-BUTYLESTERHCL;L-NORVALINET-BUTYLESTERHYDROCHLORIDE;L-Norvalinetert-butylesterhydrochloride;H-NVA-OTBUHCL;L-Norvalinetert-butylhydrochloride;(S)-tert-butyl2-aminopentanoatehydrochloride;L-2-AMinovalericacid-t-butylester·HCl
Application
L-Norvaline tert-butyl ester hydrochloride is a potential useful chemical compound, which has applications in organic synthesis and drug discovery.
Firstly, L-Norvaline tert-butyl ester hydrochloride can serve as a synthetic intermediate, contributing to the synthesis of other organic compounds. Due to its specific chemical structure and properties, L-Norvaline tert-butyl ester hydrochloride is used as a key synthetic unit in synthetic biology and medicinal chemistry. By reacting with other organic molecules, it can be employed in the synthesis of compounds with specific structures and functions, which can be further utilized in research, drug development, or production of other valuable chemicals.
Secondly, L-Norvaline tert-butyl ester hydrochloride can also act as a chiral auxiliary agent for the synthesis of organic molecules with specific stereochemistry. Chirality is an essential property of many organic molecules, determining their biological activity and functionality. By utilizing L-Norvaline tert-butyl ester hydrochloride as a chiral auxiliary agent, the stereochemistry of organic molecules can be controlled, leading to the synthesis of organic compounds with desired optical activity. These optically active compounds have a wide range of applications in drug discovery, chemical synthesis, and materials science.
Additionally, L-Norvaline tert-butyl ester hydrochloride can be employed in peptide synthesis. In peptide synthesis, the stereochemistry of amino acids is crucial for the biological activity and stability of peptides. L-Norvaline tert-butyl ester hydrochloride, serving as a derivative of amino acid with stereochemical protection, can play a key role in peptide synthesis, enhancing the stability and biological activity of peptides.
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