(S)-3-((tert-Butoxycarbonyl)amino)-3-(thiophen-2-yl)propanoic acid

95%

Reagent Code: #233324
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CAS Number 500770-66-1

science Other reagents with same CAS 500770-66-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.33 g/mol
Formula C₁₂H₁₇NO₄S
badge Registry Numbers
MDL Number MFCD03427912
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for peptide mimetics and structure-activity relationship studies. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to the Boc-protected amine and carboxylic acid handle for coupling. The thiophene ring can enhance binding affinity in drug candidates through π-π interactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,710.00
inventory 250mg
10-20 days ฿9,700.00
(S)-3-((tert-Butoxycarbonyl)amino)-3-(thiophen-2-yl)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for peptide mimetics and structure-activity relationship studies. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to the Boc-protected amine and carboxylic acid handle for coupling. The thiophene ring can enhance binding affinity in drug candidates thro
Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for peptide mimetics and structure-activity relationship studies. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to the Boc-protected amine and carboxylic acid handle for coupling. The thiophene ring can enhance binding affinity in drug candidates through π-π interactions.
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