4-Bromo-N-isopropylbenzenesulfonamide

95%

Reagent Code: #150289
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CAS Number 1984-27-6

science Other reagents with same CAS 1984-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.17 g/mol
Formula C₉H₁₂BrNO₂S
badge Registry Numbers
MDL Number MFCD01215090
thermostat Physical Properties
Melting Point 87-89 °C
Boiling Point 348.4±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.467±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in organic synthesis, enabling the introduction of sulfonyl groups into larger molecules. Its bromo substituent allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in the preparation of kinase inhibitors and other biologically active agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,110.00
inventory 1g
10-20 days ฿2,670.00
inventory 5g
10-20 days ฿9,330.00

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4-Bromo-N-isopropylbenzenesulfonamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in organic synthesis, enabling the introduction of sulfonyl groups into larger molecules. Its bromo substituent allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in the preparatio

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in organic synthesis, enabling the introduction of sulfonyl groups into larger molecules. Its bromo substituent allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in the preparation of kinase inhibitors and other biologically active agents.

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