(R)-tert-Butyl 2-(methylamino)propanoate hydrochloride

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Reagent Code: #230160
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CAS Number 405513-14-6

science Other reagents with same CAS 405513-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.69 g/mol
Formula C₈H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD08275767
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and ester functionalities make it suitable for peptide-like structures and beta-amino acid derivatives. Commonly employed in the preparation of central nervous system agents and cardiovascular drugs where the (R)-enantiomer provides desired biological activity. The hydrochloride salt form enhances stability and handling during multi-step syntheses.

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inventory 5g
10-20 days ฿28,800.00

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(R)-tert-Butyl 2-(methylamino)propanoate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and ester functionalities make it suitable for peptide-like structures and beta-amino acid derivatives. Commonly employed in the preparation of central nervous system agents and cardiovascular drugs where the (R)-enantiomer provides desired biological activity. The hydrochloride salt form enhances stability

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and ester functionalities make it suitable for peptide-like structures and beta-amino acid derivatives. Commonly employed in the preparation of central nervous system agents and cardiovascular drugs where the (R)-enantiomer provides desired biological activity. The hydrochloride salt form enhances stability and handling during multi-step syntheses.

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