Rel-(1R,2R)-2-[[(1,1-Dimethylethoxy)Carbonyl]Amino]Cyclopropanecarboxylic Acid

97%

Reagent Code: #231530
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CAS Number 1212381-16-2

science Other reagents with same CAS 1212381-16-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 402.44 g/mol
Formula C₁₈H₃₀N₂O₈
inventory_2 Storage & Handling
Storage Room temperature

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 compounds. Its cyclopropane structure with defined stereochemistry allows for rigid conformation in drug design, enhancing selectivity and metabolic stability. Commonly employed in peptide mimetics and as an intermediate in the preparation of antiviral and anticancer agents. The Boc-protected amine group enables easy incorporation into larger molecular frameworks using standard coupling techniques in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,230.00
inventory 100mg
10-20 days ฿9,350.00
inventory 250mg
10-20 days ฿16,400.00
inventory 500mg
10-20 days ฿30,540.00
inventory 1g
10-20 days ฿50,900.00
Rel-(1R,2R)-2-[[(1,1-Dimethylethoxy)Carbonyl]Amino]Cyclopropanecarboxylic Acid
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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 compounds. Its cyclopropane structure with defined stereochemistry allows for rigid conformation in drug design, enhancing selectivity and metabolic stability. Commonly employed in peptide mimetics and as an intermediate in the preparation of antiviral and anticancer agents. The Boc-protected amine group enables easy incorporation into larger molecular

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its cyclopropane structure with defined stereochemistry allows for rigid conformation in drug design, enhancing selectivity and metabolic stability. Commonly employed in peptide mimetics and as an intermediate in the preparation of antiviral and anticancer agents. The Boc-protected amine group enables easy incorporation into larger molecular frameworks using standard coupling techniques in organic synthesis.

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