(R)-Methyl2-amino-3-((tert-butoxycarbonyl)amino)propanoatehydrochloride

98%

Reagent Code: #232156
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CAS Number 919792-96-4

science Other reagents with same CAS 919792-96-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.71 g/mol
Formula C₉H₁₉ClN₂O₄
badge Registry Numbers
MDL Number MFCD05663450
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and peptide-based drugs. Its protected amine and carboxylate groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where stereochemistry is critical for biological activity. Also utilized in research settings for the construction of complex molecules requiring enantiomerically pure intermediates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,550.00
inventory 250mg
10-20 days ฿5,890.00
inventory 1g
10-20 days ฿11,790.00
inventory 5g
10-20 days ฿44,560.00
inventory 10g
10-20 days ฿83,460.00
(R)-Methyl2-amino-3-((tert-butoxycarbonyl)amino)propanoatehydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and peptide-based drugs. Its protected amine and carboxylate groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where stereochemistry is critical for biological activity. Also utilized in research settings for the construction of complex molecules requiring enantiomerically pure inter

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and peptide-based drugs. Its protected amine and carboxylate groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where stereochemistry is critical for biological activity. Also utilized in research settings for the construction of complex molecules requiring enantiomerically pure intermediates.

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