5-Bromothiophen-3-amine hydrobromide

98%

Reagent Code: #153120
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CAS Number 2173992-08-8

science Other reagents with same CAS 2173992-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.96 g/mol
Formula C₄H₅Br₂NS
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MDL Number MFCD31617954
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its functional groups enable coupling reactions in medicinal chemistry, making it valuable for creating drug candidates with enhanced metabolic stability and receptor selectivity. Also employed in materials science for constructing conductive polymers and organic semiconductors due to the electron-rich nature of the thiophene ring. The hydrobromide salt form improves stability and handling during synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,850.00
inventory 250mg
10-20 days ฿6,390.00
inventory 1g
10-20 days ฿20,610.00

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5-Bromothiophen-3-amine hydrobromide
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its functional groups enable coupling reactions in medicinal chemistry, making it valuable for creating drug candidates with enhanced metabolic stability and receptor selectivity. Also employed in materials science for constructing conductive polymers and organic semiconductors due to the electron-rich nature of the thiophene ring. The hydrobromide salt

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its functional groups enable coupling reactions in medicinal chemistry, making it valuable for creating drug candidates with enhanced metabolic stability and receptor selectivity. Also employed in materials science for constructing conductive polymers and organic semiconductors due to the electron-rich nature of the thiophene ring. The hydrobromide salt form improves stability and handling during synthetic processes.

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