(S)-tert-Butyl 2-amino-3-methoxypropanoate hydrochloride

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Reagent Code: #38285
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CAS Number 1821839-04-6

science Other reagents with same CAS 1821839-04-6

blur_circular Chemical Specifications

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Weight 211.6864 g/mol
Formula C₈H₁₈ClNO₃
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the production of chiral molecules. Its structure, featuring both an amino group and a methoxy group, makes it a valuable building block for creating complex organic compounds. It is often employed in the development of drugs targeting neurological disorders, as the chiral center allows for the creation of enantiomerically pure substances, which are crucial for effective and safe medications. Additionally, it is utilized in peptide chemistry for modifying peptide chains to enhance their stability or biological activity. Its hydrochloride form improves solubility, facilitating its use in various chemical reactions.

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inventory 1g
10-20 days ฿4,680.00

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(S)-tert-Butyl 2-amino-3-methoxypropanoate hydrochloride
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the production of chiral molecules. Its structure, featuring both an amino group and a methoxy group, makes it a valuable building block for creating complex organic compounds. It is often employed in the development of drugs targeting neurological disorders, as the chiral center allows for the creation of enantiomerically pure substances, which are crucial for effective and safe medications. Additionally, i

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the production of chiral molecules. Its structure, featuring both an amino group and a methoxy group, makes it a valuable building block for creating complex organic compounds. It is often employed in the development of drugs targeting neurological disorders, as the chiral center allows for the creation of enantiomerically pure substances, which are crucial for effective and safe medications. Additionally, it is utilized in peptide chemistry for modifying peptide chains to enhance their stability or biological activity. Its hydrochloride form improves solubility, facilitating its use in various chemical reactions.

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