(1R,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid

95%

Reagent Code: #230102
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CAS Number 161660-94-2

science Other reagents with same CAS 161660-94-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
thermostat Physical Properties
Melting Point 96.1°C
Boiling Point 382.5°C
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 biologically active compounds where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities allow for selective coupling reactions, making it valuable in peptide synthesis and medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the constrained cyclopentane scaffold, which can enhance metabolic stability and target selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿154.00
inventory 1g
10-20 days ฿650.00
inventory 5g
10-20 days ฿2,980.00
inventory 100g
10-20 days ฿51,930.00
inventory 25g
10-20 days ฿13,370.00
(1R,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities allow for selective coupling reactions, making it valuable in peptide synthesis and medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the constrained cyclopentane scaffold, which can enhance metabolic stability and

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities allow for selective coupling reactions, making it valuable in peptide synthesis and medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the constrained cyclopentane scaffold, which can enhance metabolic stability and target selectivity.

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