4-Bromo-N-(pyridin-3-yl)benzenesulfonamide

95%

Reagent Code: #215709
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CAS Number 3665-12-1

science Other reagents with same CAS 3665-12-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.17 g/mol
Formula C₁₁H₉BrN₂O₂S
badge Registry Numbers
MDL Number MFCD01215111
thermostat Physical Properties
Melting Point 187-188 °C
Boiling Point 445.7±51.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.666±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anticancer activity. It serves as a building block in medicinal chemistry for constructing kinase inhibitors and other biologically active molecules. Its bromo functional group allows for further modification via cross-coupling reactions, enabling the creation of diverse compound libraries for drug discovery. Also employed in research settings to design and study new therapeutic agents targeting specific enzymes and receptors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,480.00
inventory 250mg
10-20 days ฿2,520.00
inventory 1g
10-20 days ฿7,320.00

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4-Bromo-N-(pyridin-3-yl)benzenesulfonamide
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anticancer activity. It serves as a building block in medicinal chemistry for constructing kinase inhibitors and other biologically active molecules. Its bromo functional group allows for further modification via cross-coupling reactions, enabling the creation of diverse compound libraries for drug discovery. Also employed in research settings to design and stud

Used as an intermediate in pharmaceutical synthesis, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anticancer activity. It serves as a building block in medicinal chemistry for constructing kinase inhibitors and other biologically active molecules. Its bromo functional group allows for further modification via cross-coupling reactions, enabling the creation of diverse compound libraries for drug discovery. Also employed in research settings to design and study new therapeutic agents targeting specific enzymes and receptors.

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