3-amino-N-(2-methoxyphenyl)-Benzenesulfonamide

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Reagent Code: #245703
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CAS Number 327093-01-6

science Other reagents with same CAS 327093-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.33 g/mol
Formula C₁₃H₁₄N₂O₃S
badge Registry Numbers
MDL Number MFCD02708235
thermostat Physical Properties
Boiling Point 487.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.358±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. Exhibits potential in the design of enzyme inhibitors due to the presence of primary amine and sulfonamide functional groups. Applied in medicinal chemistry research for constructing libraries of compounds targeting carbonic anhydrase and other metalloenzymes, with applications in treating conditions such as glaucoma, cancer, and metabolic acidosis. Also utilized in the preparation of dyes and functional materials where aromatic sulfonamides contribute to stability and binding properties.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,860.00
inventory 5mg
10-20 days ฿4,530.00

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3-amino-N-(2-methoxyphenyl)-Benzenesulfonamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. Exhibits potential in the design of enzyme inhibitors due to the presence of primary amine and sulfonamide functional groups. Applied in medicinal chemistry research for constructing libraries of compounds targeting carbonic anhydrase and other metalloenzymes, with applications in treating conditions such as glaucoma, cancer, and metabolic acidosis. Also utilize

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. Exhibits potential in the design of enzyme inhibitors due to the presence of primary amine and sulfonamide functional groups. Applied in medicinal chemistry research for constructing libraries of compounds targeting carbonic anhydrase and other metalloenzymes, with applications in treating conditions such as glaucoma, cancer, and metabolic acidosis. Also utilized in the preparation of dyes and functional materials where aromatic sulfonamides contribute to stability and binding properties.

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