(R)-4-tert-Butyl 1-methyl 2-aminosuccinate

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Reagent Code: #231483
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CAS Number 84907-98-2

science Other reagents with same CAS 84907-98-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.24 g/mol
Formula C₉H₁₇NO₄
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its enantiomerically pure structure makes it valuable for asymmetric synthesis, where stereochemistry is critical for drug efficacy. Commonly employed in the preparation of intermediates for antiviral and anticancer agents. The tert-butyl and methyl ester groups provide favorable solubility and protection during multi-step syntheses, allowing selective deprotection and further functionalization.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,810.00
5g
10-20 days ฿7,790.00
25g
10-20 days ฿25,180.00
(R)-4-tert-Butyl 1-methyl 2-aminosuccinate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its enantiomerically pure structure makes it valuable for asymmetric synthesis, where stereochemistry is critical for drug efficacy. Commonly employed in the preparation of intermediates for antiviral and anticancer agents. The tert-butyl and methyl ester groups provide favorable solubility and protection during multi-step syntheses, allowing

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its enantiomerically pure structure makes it valuable for asymmetric synthesis, where stereochemistry is critical for drug efficacy. Commonly employed in the preparation of intermediates for antiviral and anticancer agents. The tert-butyl and methyl ester groups provide favorable solubility and protection during multi-step syntheses, allowing selective deprotection and further functionalization.

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