N-tert-Butyl 5-bromo-2-thiophenesulfonamide

97%

Reagent Code: #217263
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CAS Number 286932-39-6

science Other reagents with same CAS 286932-39-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.22 g/mol
Formula C₈H₁₂BrNO₂S₂
thermostat Physical Properties
Melting Point 62°C
Boiling Point 366.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and fungicides, due to its ability to selectively modify bioactive molecules. Its sulfonamide group enhances binding affinity in biologically active compounds, making it valuable in crop protection chemistry. Also employed in medicinal chemistry research for developing heterocyclic compounds with potential pharmacological activity. The bromine atom allows for further functionalization via cross-coupling reactions, enabling the construction of complex molecular architectures in both agricultural and pharmaceutical applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿410.00
5g
10-20 days ฿800.00
N-tert-Butyl 5-bromo-2-thiophenesulfonamide
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and fungicides, due to its ability to selectively modify bioactive molecules. Its sulfonamide group enhances binding affinity in biologically active compounds, making it valuable in crop protection chemistry. Also employed in medicinal chemistry research for developing heterocyclic compounds with potential pharmacological activity. The bromine atom allows for further functionalization via cross-coupling reactions, enabl

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and fungicides, due to its ability to selectively modify bioactive molecules. Its sulfonamide group enhances binding affinity in biologically active compounds, making it valuable in crop protection chemistry. Also employed in medicinal chemistry research for developing heterocyclic compounds with potential pharmacological activity. The bromine atom allows for further functionalization via cross-coupling reactions, enabling the construction of complex molecular architectures in both agricultural and pharmaceutical applications.

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