(R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)azetidine-2-carboxylic acid

96%

Reagent Code: #230123
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CAS Number 374791-02-3

science Other reagents with same CAS 374791-02-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.34 g/mol
Formula C₁₉H₁₇NO₄
thermostat Physical Properties
Boiling Point 543.3°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals and bioactive molecules. Its azetidine ring provides structural rigidity, enhancing metabolic stability and influencing conformational preferences in peptide analogs. The Fmoc group allows for solid-phase peptide synthesis, enabling stepwise assembly of complex peptides. Commonly employed in medicinal chemistry for developing enzyme inhibitors and receptor modulators, particularly where stereochemistry plays a critical role in biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿730.00
1g
10-20 days ฿2,640.00
5g
10-20 days ฿11,440.00
(R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)azetidine-2-carboxylic acid
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Used as a chiral building block in the synthesis of peptide-based pharmaceuticals and bioactive molecules. Its azetidine ring provides structural rigidity, enhancing metabolic stability and influencing conformational preferences in peptide analogs. The Fmoc group allows for solid-phase peptide synthesis, enabling stepwise assembly of complex peptides. Commonly employed in medicinal chemistry for developing enzyme inhibitors and receptor modulators, particularly where stereochemistry plays a critical role

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals and bioactive molecules. Its azetidine ring provides structural rigidity, enhancing metabolic stability and influencing conformational preferences in peptide analogs. The Fmoc group allows for solid-phase peptide synthesis, enabling stepwise assembly of complex peptides. Commonly employed in medicinal chemistry for developing enzyme inhibitors and receptor modulators, particularly where stereochemistry plays a critical role in biological activity.

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