N-Methyl-N-[(2S)-oxiran-2-yl]methylmethanesulfonamide

95%

Reagent Code: #218815
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CAS Number 866777-98-2

science Other reagents with same CAS 866777-98-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.21 g/mol
Formula C₅H₁₁NO₃S
badge Registry Numbers
MDL Number MFCD30803369
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its epoxide functionality allows for ring-opening reactions with nucleophiles, enabling the formation of complex amine or alcohol derivatives. Commonly employed in the preparation of protease inhibitors and other bioactive molecules due to its ability to mimic transition states in enzymatic reactions. Also utilized in agrochemical synthesis for creating enantiomerically pure compounds. Its sulfonamide group enhances stability and influences solubility, making it suitable for multistep organic transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,930.00
inventory 1g
10-20 days ฿3,070.00
inventory 5g
10-20 days ฿14,840.00
N-Methyl-N-[(2S)-oxiran-2-yl]methylmethanesulfonamide
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its epoxide functionality allows for ring-opening reactions with nucleophiles, enabling the formation of complex amine or alcohol derivatives. Commonly employed in the preparation of protease inhibitors and other bioactive molecules due to its ability to mimic transition states in enzymatic reactions. Also utilized in ag
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its epoxide functionality allows for ring-opening reactions with nucleophiles, enabling the formation of complex amine or alcohol derivatives. Commonly employed in the preparation of protease inhibitors and other bioactive molecules due to its ability to mimic transition states in enzymatic reactions. Also utilized in agrochemical synthesis for creating enantiomerically pure compounds. Its sulfonamide group enhances stability and influences solubility, making it suitable for multistep organic transformations.
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