3-Bromo-4-methylbenzenesulfonamide

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Reagent Code: #156018
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CAS Number 210824-69-4

science Other reagents with same CAS 210824-69-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.11 g/mol
Formula C₇H₈BrNO₂S
badge Registry Numbers
MDL Number MFCD09801033
thermostat Physical Properties
Boiling Point 379 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in organic synthesis for introducing the 3-bromo-4-methylbenzenesulfonyl group, which can enhance the biological activity or stability of target molecules. Also employed in the preparation of agrochemicals and functional materials where sulfonyl derivatives are required. Its bromo functionality allows for further cross-coupling reactions, enabling the construction of more complex molecular architectures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,860.00
inventory 5g
10-20 days ฿24,690.00
inventory 1g
10-20 days ฿5,740.00

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3-Bromo-4-methylbenzenesulfonamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in organic synthesis for introducing the 3-bromo-4-methylbenzenesulfonyl group, which can enhance the biological activity or stability of target molecules. Also employed in the preparation of agrochemicals and functional materials where sulfonyl derivatives are required. Its bromo functionality allows for

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in organic synthesis for introducing the 3-bromo-4-methylbenzenesulfonyl group, which can enhance the biological activity or stability of target molecules. Also employed in the preparation of agrochemicals and functional materials where sulfonyl derivatives are required. Its bromo functionality allows for further cross-coupling reactions, enabling the construction of more complex molecular architectures.

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