N-tert-Butylbenzenesulfonamide

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Reagent Code: #218804
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CAS Number 2512-24-5

science Other reagents with same CAS 2512-24-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.30 g/mol
Formula C₁₀H₁₅NO₂S
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MDL Number MFCD00462465
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals and agrochemicals. It serves as a building block in the development of biologically active compounds due to its stability and reactivity profile. The compound is also employed in research settings for the design of novel enzyme inhibitors, where the tert-butyl group can influence binding affinity and metabolic stability. Its role as a protecting group or directing agent in synthetic routes further enhances its utility in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,420.00
inventory 5g
10-20 days ฿4,600.00
inventory 10g
10-20 days ฿7,930.00

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N-tert-Butylbenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals and agrochemicals. It serves as a building block in the development of biologically active compounds due to its stability and reactivity profile. The compound is also employed in research settings for the design of novel enzyme inhibitors, where the tert-butyl group can influence binding affinity and metabolic stability. Its role as a protecting group or directing agent in synthetic routes f

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals and agrochemicals. It serves as a building block in the development of biologically active compounds due to its stability and reactivity profile. The compound is also employed in research settings for the design of novel enzyme inhibitors, where the tert-butyl group can influence binding affinity and metabolic stability. Its role as a protecting group or directing agent in synthetic routes further enhances its utility in complex molecule assembly.

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