2-(p-Tolylsulfonyl)-6-thia-2-azaspiro[2.5]octane

95%

Reagent Code: #75164
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CAS Number 1207754-86-6

science Other reagents with same CAS 1207754-86-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.41 g/mol
Formula C₁₃H₁₇NO₂S₂
badge Registry Numbers
MDL Number MFCD22123258
inventory_2 Storage & Handling
Storage Room temperature, sealed, ventilated

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecular structures. Its unique spirocyclic framework makes it valuable in the design and synthesis of bioactive compounds, particularly in pharmaceutical research. It is often employed in the construction of heterocyclic compounds, which are essential in the development of drugs targeting various diseases. Additionally, its sulfonyl and thia groups contribute to its reactivity, enabling its use in cross-coupling reactions and as a building block for creating molecules with potential therapeutic applications. Its role in medicinal chemistry is significant, particularly in the exploration of new drug candidates with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿122,550.00
inventory 1g
10-20 days ฿283,850.00

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2-(p-Tolylsulfonyl)-6-thia-2-azaspiro[2.5]octane
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This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecular structures. Its unique spirocyclic framework makes it valuable in the design and synthesis of bioactive compounds, particularly in pharmaceutical research. It is often employed in the construction of heterocyclic compounds, which are essential in the development of drugs targeting various diseases. Additionally, its sulfonyl and thia groups contribute to its reactivity, enabling its use

This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecular structures. Its unique spirocyclic framework makes it valuable in the design and synthesis of bioactive compounds, particularly in pharmaceutical research. It is often employed in the construction of heterocyclic compounds, which are essential in the development of drugs targeting various diseases. Additionally, its sulfonyl and thia groups contribute to its reactivity, enabling its use in cross-coupling reactions and as a building block for creating molecules with potential therapeutic applications. Its role in medicinal chemistry is significant, particularly in the exploration of new drug candidates with improved efficacy and selectivity.

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