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

≥98%

Reagent Code: #59019
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CAS Number 141699-56-1

science Other reagents with same CAS 141699-56-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.35 g/mol
Formula C₁₁H₂₁NO₅S
badge Registry Numbers
MDL Number MFCD04038482
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring a pyrrolidine ring and a sulfonate ester group, makes it suitable for various chemical transformations, particularly in the development of pharmaceuticals and bioactive compounds. The tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step syntheses. Additionally, the methylsulfonyloxy (mesylate) group serves as a good leaving group, facilitating nucleophilic substitution reactions to introduce new functional groups. This chemical is often employed in the synthesis of alkaloids, peptidomimetics, and other nitrogen-containing heterocycles, which are essential in drug discovery and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,692.00
inventory 100mg
10-20 days ฿7,128.00
inventory 1g
10-20 days ฿34,092.00

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tert-Butyl 3-(((methylsulfonyl)oxy)methyl)pyrrolidine-1-carboxylate
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This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring a pyrrolidine ring and a sulfonate ester group, makes it suitable for various chemical transformations, particularly in the development of pharmaceuticals and bioactive compounds. The tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step syntheses. Additionally, the methylsulfonyloxy (

This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring a pyrrolidine ring and a sulfonate ester group, makes it suitable for various chemical transformations, particularly in the development of pharmaceuticals and bioactive compounds. The tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step syntheses. Additionally, the methylsulfonyloxy (mesylate) group serves as a good leaving group, facilitating nucleophilic substitution reactions to introduce new functional groups. This chemical is often employed in the synthesis of alkaloids, peptidomimetics, and other nitrogen-containing heterocycles, which are essential in drug discovery and medicinal chemistry.

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