tert-Butyl methylsulfonylcarbamate

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Reagent Code: #148535
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CAS Number 147751-16-4

science Other reagents with same CAS 147751-16-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.24 g/mol
Formula C₆H₁₃NO₄S
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MDL Number MFCD13194912
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and carbamates. It acts as a protecting group for amines due to the stability of the tert-butyl moiety under various reaction conditions. The methylsulfonyl group enhances electrophilicity, facilitating nucleophilic attack during coupling reactions. Commonly employed in medicinal chemistry for the development of pharmaceutical intermediates where selective amine functionalization is required. Its application extends to peptide synthesis and the construction of nitrogen-containing heterocycles.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿470.00
inventory 1g
10-20 days ฿1,600.00
inventory 5g
10-20 days ฿6,030.00
inventory 10g
10-20 days ฿11,130.00

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tert-Butyl methylsulfonylcarbamate
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Used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and carbamates. It acts as a protecting group for amines due to the stability of the tert-butyl moiety under various reaction conditions. The methylsulfonyl group enhances electrophilicity, facilitating nucleophilic attack during coupling reactions. Commonly employed in medicinal chemistry for the development of pharmaceutical intermediates where selective amine functionalization is required. Its application extends t

Used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and carbamates. It acts as a protecting group for amines due to the stability of the tert-butyl moiety under various reaction conditions. The methylsulfonyl group enhances electrophilicity, facilitating nucleophilic attack during coupling reactions. Commonly employed in medicinal chemistry for the development of pharmaceutical intermediates where selective amine functionalization is required. Its application extends to peptide synthesis and the construction of nitrogen-containing heterocycles.

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