(R)-tert-Butyl 3-((methylsulfonyl)oxy)pyrrolidine-1-carboxylate

95%

Reagent Code: #230719
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CAS Number 127423-61-4

science Other reagents with same CAS 127423-61-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.33 g/mol
Formula C₁₀H₁₉NO₅S
badge Registry Numbers
MDL Number MFCD06809586
inventory_2 Storage & Handling
Storage 2-8℃, dry, sealed

description Product Description

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure allows for selective introduction of the (R)-pyrrolidine moiety, which is valuable in creating enantiomerically pure drugs. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where stereochemistry plays a critical role in activity. The methylsulfonyl group acts as a good leaving group, facilitating nucleophilic substitution reactions under mild conditions. Also utilized in asymmetric synthesis and medicinal chemistry research for constructing complex nitrogen-containing heterocycles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,320.00
inventory 5g
10-20 days ฿5,710.00
inventory 10g
10-20 days ฿9,800.00
inventory 25g
10-20 days ฿23,950.00
(R)-tert-Butyl 3-((methylsulfonyl)oxy)pyrrolidine-1-carboxylate
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Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure allows for selective introduction of the (R)-pyrrolidine moiety, which is valuable in creating enantiomerically pure drugs. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where stereochemistry plays a critical role in activity. The methylsulfonyl group acts as a good leaving group, facilitating nucleophilic substitution reac

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure allows for selective introduction of the (R)-pyrrolidine moiety, which is valuable in creating enantiomerically pure drugs. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where stereochemistry plays a critical role in activity. The methylsulfonyl group acts as a good leaving group, facilitating nucleophilic substitution reactions under mild conditions. Also utilized in asymmetric synthesis and medicinal chemistry research for constructing complex nitrogen-containing heterocycles.

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