(2S,4R)-N-Boc-trans-4-methanesulfonyloxy-L-proline

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Reagent Code: #237827
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CAS Number 202477-59-6

science Other reagents with same CAS 202477-59-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.34 g/mol
Formula C₁₁H₁₉NO₇S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. The N-Boc group protects the nitrogen, while the free carboxylic acid and methanesulfonyloxy (mesylate) at the 4-position allow selective reactions at specific sites, making it valuable in multi-step organic syntheses. The mesylate group serves as a good leaving group, enabling nucleophilic substitution reactions to introduce various side chains, such as carbon-carbon or carbon-nitrogen bonds. Commonly employed in the preparation of peptide mimetics and cyclic amino acid derivatives for drug discovery research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,250.00
inventory 250mg
10-20 days ฿7,080.00
inventory 1g
10-20 days ฿14,150.00
inventory 5g
10-20 days ฿49,590.00
inventory 10g
10-20 days ฿89,100.00
(2S,4R)-N-Boc-trans-4-methanesulfonyloxy-L-proline
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Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. The N-Boc group protects the nitrogen, while the free carboxylic acid and methanesulfonyloxy (mesylate) at the 4-position allow selective reactions at specific sites, making it valuable in multi-step organic syntheses. The mesylate group serves as a good leaving group, enabling nucleophilic substitution reactions to introduce vario

Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. The N-Boc group protects the nitrogen, while the free carboxylic acid and methanesulfonyloxy (mesylate) at the 4-position allow selective reactions at specific sites, making it valuable in multi-step organic syntheses. The mesylate group serves as a good leaving group, enabling nucleophilic substitution reactions to introduce various side chains, such as carbon-carbon or carbon-nitrogen bonds. Commonly employed in the preparation of peptide mimetics and cyclic amino acid derivatives for drug discovery research.

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