ethyl3-bromo-4H-furo[3,2-b]pyrrole-5-carboxylate

≥95%

Reagent Code: #65123
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CAS Number 332099-50-0

science Other reagents with same CAS 332099-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.07 g/mol
Formula C₉H₈BrNO₃
badge Registry Numbers
MDL Number MFCD16657716
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique furopyrrole framework makes it valuable in the synthesis of heterocyclic compounds, which are often explored for their potential biological activities. Researchers leverage its reactive bromine and ester functional groups to facilitate further chemical modifications, such as cross-coupling reactions or nucleophilic substitutions. This enables the creation of diverse derivatives that can be screened for pharmaceutical applications, particularly in the design of drug candidates targeting specific enzymes or receptors. Additionally, its structural features make it a potential candidate for materials science, where it could be incorporated into organic electronic materials or polymers with specialized properties.

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inventory 1g
10-20 days ฿44,289.00

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ethyl3-bromo-4H-furo[3,2-b]pyrrole-5-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique furopyrrole framework makes it valuable in the synthesis of heterocyclic compounds, which are often explored for their potential biological activities. Researchers leverage its reactive bromine and ester functional groups to facilitate further chemical modifications, such as cross-coupling reactions or nucleophilic substitutions. This enables the creatio

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique furopyrrole framework makes it valuable in the synthesis of heterocyclic compounds, which are often explored for their potential biological activities. Researchers leverage its reactive bromine and ester functional groups to facilitate further chemical modifications, such as cross-coupling reactions or nucleophilic substitutions. This enables the creation of diverse derivatives that can be screened for pharmaceutical applications, particularly in the design of drug candidates targeting specific enzymes or receptors. Additionally, its structural features make it a potential candidate for materials science, where it could be incorporated into organic electronic materials or polymers with specialized properties.

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