5-Bromo-N,N-diethylpyridine-3-sulfonamide

95%

Reagent Code: #154535
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CAS Number 62009-37-4

science Other reagents with same CAS 62009-37-4

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scatter_plot Molecular Information
Weight 293.18 g/mol
Formula C₉H₁₃BrN₂O₂S
badge Registry Numbers
MDL Number MFCD09475859
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry for modifying pyridine derivatives to enhance biological activity. Also employed in research settings to explore new bioactive molecules and in the preparation of receptor ligands for biochemical assays. Its bromine functionality allows for further cross-coupling reactions, enabling diverse chemical modifications in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,860.00
inventory 5g
10-20 days ฿36,520.00

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5-Bromo-N,N-diethylpyridine-3-sulfonamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry for modifying pyridine derivatives to enhance biological activity. Also employed in research settings to explore new bioactive molecules and in the preparation of receptor ligands for biochemical assays. Its bromine functionality allows for further cross-coupling rea
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry for modifying pyridine derivatives to enhance biological activity. Also employed in research settings to explore new bioactive molecules and in the preparation of receptor ligands for biochemical assays. Its bromine functionality allows for further cross-coupling reactions, enabling diverse chemical modifications in drug discovery programs.
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