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.

Available Sizes & Pricing

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