6-Tosyl-6-azabicyclo[3.1.0]hexane

95%

Reagent Code: #242023
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CAS Number 81097-48-5

science Other reagents with same CAS 81097-48-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.32 g/mol
Formula C₁₂H₁₅NO₂S
badge Registry Numbers
MDL Number MFCD02852961
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its strained bicyclic structure and reactive tosyl group make it valuable for ring-opening and functionalization reactions. Commonly employed in the preparation of pyrrolidine-based drug candidates, including those with antiviral and neuromodulatory properties. Also utilized in asymmetric synthesis due to its rigid scaffold, enabling selective formation of stereoisomers in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,600.00
inventory 250mg
10-20 days ฿16,000.00

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6-Tosyl-6-azabicyclo[3.1.0]hexane
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its strained bicyclic structure and reactive tosyl group make it valuable for ring-opening and functionalization reactions. Commonly employed in the preparation of pyrrolidine-based drug candidates, including those with antiviral and neuromodulatory properties. Also utilized in asymmetric synthesis due to its rigid scaffold, enabling selective formation

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its strained bicyclic structure and reactive tosyl group make it valuable for ring-opening and functionalization reactions. Commonly employed in the preparation of pyrrolidine-based drug candidates, including those with antiviral and neuromodulatory properties. Also utilized in asymmetric synthesis due to its rigid scaffold, enabling selective formation of stereoisomers in medicinal chemistry research.

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