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

97%

Reagent Code: #230197
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CAS Number 489446-85-7

science Other reagents with same CAS 489446-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
thermostat Physical Properties
Melting Point 117.3°C
Boiling Point 382.5±31.0°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 protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective interactions in drug design, enhancing potency and reducing side effects. Commonly employed in peptide mimetics and as an intermediate in the preparation of cyclopentane-based scaffolds for antiviral and central nervous system agents. The Boc-protected amine group enables easy deprotection and further functionalization in multi-step organic syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,960.00
250mg
10-20 days ฿3,170.00
5g
10-20 days ฿40,960.00
1g
10-20 days ฿10,240.00
(1R,3R)-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 protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective interactions in drug design, enhancing potency and reducing side effects. Commonly employed in peptide mimetics and as an intermediate in the preparation of cyclopentane-based scaffolds for antiviral and central nervous system agents. The Boc-protected amine group enables easy deprotection and further functional

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective interactions in drug design, enhancing potency and reducing side effects. Commonly employed in peptide mimetics and as an intermediate in the preparation of cyclopentane-based scaffolds for antiviral and central nervous system agents. The Boc-protected amine group enables easy deprotection and further functionalization in multi-step organic syntheses.

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