2-Benzyl-6-tosyl-2,6-diazaspiro[3.3]heptane

98%

Reagent Code: #75352
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CAS Number 1041026-64-5

science Other reagents with same CAS 1041026-64-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.46 g/mol
Formula C₁₉H₂₂N₂O₂S
badge Registry Numbers
MDL Number MFCD13180713
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its unique spirocyclic structure makes it a valuable scaffold for developing potential drug candidates, particularly in the area of central nervous system (CNS) disorders. Researchers often employ it in the design of compounds targeting receptors or enzymes involved in neurological pathways. Additionally, its tosyl group provides a reactive site for further chemical modifications, enabling the creation of diverse derivatives for pharmacological screening. Its application extends to the development of novel therapeutic agents with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿25,146.00
inventory 1g
10-20 days ฿50,292.00

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2-Benzyl-6-tosyl-2,6-diazaspiro[3.3]heptane
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its unique spirocyclic structure makes it a valuable scaffold for developing potential drug candidates, particularly in the area of central nervous system (CNS) disorders. Researchers often employ it in the design of compounds targeting receptors or enzymes involved in neurological pathways. Additionally, its tosyl group provides a reactive site for furt

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its unique spirocyclic structure makes it a valuable scaffold for developing potential drug candidates, particularly in the area of central nervous system (CNS) disorders. Researchers often employ it in the design of compounds targeting receptors or enzymes involved in neurological pathways. Additionally, its tosyl group provides a reactive site for further chemical modifications, enabling the creation of diverse derivatives for pharmacological screening. Its application extends to the development of novel therapeutic agents with improved efficacy and selectivity.

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