2-Butyl-5-nitrobenzofuran

98%

Reagent Code: #42233
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CAS Number 133238-87-6

science Other reagents with same CAS 133238-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.24 g/mol
Formula C₁₂H₁₃NO₃
badge Registry Numbers
MDL Number MFCD14525624
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

2-Butyl-5-nitrobenzofuran is primarily used as a key intermediate in organic synthesis within the pharmaceutical industry. It plays a crucial role in the production of dronedarone, an antiarrhythmic agent employed in the treatment of atrial fibrillation and other cardiovascular disorders. The compound's benzofuran core with a nitro substituent enables the creation of derivatives with targeted pharmacological activities, such as modulation of ion channels. In research settings, it is also utilized for exploring reaction mechanisms in nitroaromatic chemistry and developing novel therapeutic agents.

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Test Parameter Specification
Appearance White to Yellow to Brown solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50g
10-20 days ฿15,760.00
inventory 10g
10-20 days ฿3,880.00

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2-Butyl-5-nitrobenzofuran
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2-Butyl-5-nitrobenzofuran is primarily used as a key intermediate in organic synthesis within the pharmaceutical industry. It plays a crucial role in the production of dronedarone, an antiarrhythmic agent employed in the treatment of atrial fibrillation and other cardiovascular disorders. The compound's benzofuran core with a nitro substituent enables the creation of derivatives with targeted pharmacological activities, such as modulation of ion channels. In research settings, it is also utilized for exp

2-Butyl-5-nitrobenzofuran is primarily used as a key intermediate in organic synthesis within the pharmaceutical industry. It plays a crucial role in the production of dronedarone, an antiarrhythmic agent employed in the treatment of atrial fibrillation and other cardiovascular disorders. The compound's benzofuran core with a nitro substituent enables the creation of derivatives with targeted pharmacological activities, such as modulation of ion channels. In research settings, it is also utilized for exploring reaction mechanisms in nitroaromatic chemistry and developing novel therapeutic agents.

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