4-Bromo-N-tert-butylbenzenesulfonamide

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Reagent Code: #151925
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CAS Number 93281-65-3

science Other reagents with same CAS 93281-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.19 g/mol
Formula C₁₀H₁₄BrNO₂S
badge Registry Numbers
MDL Number MFCD00458267
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a building block for creating biologically active compounds, including potential antidiabetic and antimicrobial agents. The presence of the bromo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic structures. Its tert-butyl group contributes to steric stability and influences solubility, making it useful in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study structure-activity relationships in enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿700.00
inventory 250mg
10-20 days ฿1,350.00
inventory 1g
10-20 days ฿3,500.00

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4-Bromo-N-tert-butylbenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a building block for creating biologically active compounds, including potential antidiabetic and antimicrobial agents. The presence of the bromo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic structures. Its tert-butyl group contributes to steric stability and influences so

Used as an intermediate in organic synthesis, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a building block for creating biologically active compounds, including potential antidiabetic and antimicrobial agents. The presence of the bromo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic structures. Its tert-butyl group contributes to steric stability and influences solubility, making it useful in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study structure-activity relationships in enzyme inhibitors.

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