1-(Mesitylsulfonyl)pyrrolidin-2-one

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Reagent Code: #129116
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CAS Number 298193-11-0

science Other reagents with same CAS 298193-11-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.34 g/mol
Formula C₁₃H₁₇NO₃S
thermostat Physical Properties
Boiling Point 411.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.258±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key reagent in organic synthesis, particularly in the preparation of sulfonamide derivatives and heterocyclic compounds. It serves as a mesitylsulfonyl (MesSO₂) protecting or activating group in peptide synthesis and medicinal chemistry. Its stability and reactivity make it suitable for facilitating nucleophilic substitution reactions, especially in the development of pharmaceutical intermediates. Commonly employed in research settings for modifying amine functionalities and enhancing reaction selectivity under mild conditions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,520.00
inventory 100mg
10-20 days ฿44,790.00

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1-(Mesitylsulfonyl)pyrrolidin-2-one
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Used as a key reagent in organic synthesis, particularly in the preparation of sulfonamide derivatives and heterocyclic compounds. It serves as a mesitylsulfonyl (MesSO₂) protecting or activating group in peptide synthesis and medicinal chemistry. Its stability and reactivity make it suitable for facilitating nucleophilic substitution reactions, especially in the development of pharmaceutical intermediates. Commonly employed in research settings for modifying amine functionalities and enhancing reaction

Used as a key reagent in organic synthesis, particularly in the preparation of sulfonamide derivatives and heterocyclic compounds. It serves as a mesitylsulfonyl (MesSO₂) protecting or activating group in peptide synthesis and medicinal chemistry. Its stability and reactivity make it suitable for facilitating nucleophilic substitution reactions, especially in the development of pharmaceutical intermediates. Commonly employed in research settings for modifying amine functionalities and enhancing reaction selectivity under mild conditions.

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