6-[(4-methylphenyl)sulfonyl]-2-thia-6-azaspiro[3.3]heptane

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Reagent Code: #75689
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CAS Number 1233142-91-0

science Other reagents with same CAS 1233142-91-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.383 g/mol
Formula C₁₂H₁₅NO₂S₂
badge Registry Numbers
MDL Number MFCD21092023
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds. Its unique spirocyclic structure makes it valuable for designing molecules with specific conformational properties, which can enhance drug efficacy and selectivity. Additionally, it is employed in the study of enzyme inhibitors and receptor modulators, particularly in neurological and metabolic disorder research. Its sulfonyl group also allows for further functionalization, enabling the creation of diverse derivatives for screening and optimization in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 2.5g
10-20 days ฿117,540.00
inventory 1g
10-20 days ฿55,830.00

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6-[(4-methylphenyl)sulfonyl]-2-thia-6-azaspiro[3.3]heptane
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This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds. Its unique spirocyclic structure makes it valuable for designing molecules with specific conformational properties, which can enhance drug efficacy and selectivity. Additionally, it is employed in the study of enzyme inhibitors and receptor modulators, particularly in neurological and metabolic disorder research. It

This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds. Its unique spirocyclic structure makes it valuable for designing molecules with specific conformational properties, which can enhance drug efficacy and selectivity. Additionally, it is employed in the study of enzyme inhibitors and receptor modulators, particularly in neurological and metabolic disorder research. Its sulfonyl group also allows for further functionalization, enabling the creation of diverse derivatives for screening and optimization in drug discovery programs.

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