(R)-3-(3-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid

98%

Reagent Code: #230860
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CAS Number 501015-16-3

science Other reagents with same CAS 501015-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.2 g/mol
Formula C₁₄H₁₈BrNO₄
badge Registry Numbers
MDL Number MFCD03427962
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry allows for selective interactions in enzyme active sites, making it valuable in drug design for conditions such as viral infections or metabolic disorders. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, facilitating incorporation into complex peptide-like structures. Commonly employed in research settings for optimizing synthetic routes and improving enantiomeric purity of final drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,240.00
250mg
10-20 days ฿1,910.00
(R)-3-(3-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry allows for selective interactions in enzyme active sites, making it valuable in drug design for conditions such as viral infections or metabolic disorders. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, facilitating incorporation into complex peptide-like structures.

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry allows for selective interactions in enzyme active sites, making it valuable in drug design for conditions such as viral infections or metabolic disorders. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, facilitating incorporation into complex peptide-like structures. Commonly employed in research settings for optimizing synthetic routes and improving enantiomeric purity of final drug candidates.

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