(R)-3-(Anthracen-9-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid

≥95%

Reagent Code: #229525
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CAS Number 128050-98-6

science Other reagents with same CAS 128050-98-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.4 g/mol
Formula C₂₂H₂₃NO₄
badge Registry Numbers
MDL Number MFCD02094459
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its anthracene group enables fluorescence detection during purification and analysis, making it valuable in monitoring reaction progress and studying molecular interactions. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis where stereochemical control is critical. Also serves as an intermediate in the preparation of bioactive molecules and enzyme inhibitors due to its stable chirality and functional group compatibility.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿22,890.00
(R)-3-(Anthracen-9-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
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Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its anthracene group enables fluorescence detection during purification and analysis, making it valuable in monitoring reaction progress and studying molecular interactions. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis where stereochemical control is critical. Also serves as an intermediate in the preparation of bioactive molecules and e

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its anthracene group enables fluorescence detection during purification and analysis, making it valuable in monitoring reaction progress and studying molecular interactions. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis where stereochemical control is critical. Also serves as an intermediate in the preparation of bioactive molecules and enzyme inhibitors due to its stable chirality and functional group compatibility.

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