(E)-1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene

97%

Reagent Code: #78100
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CAS Number 131981-75-4

science Other reagents with same CAS 131981-75-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.06 g/mol
Formula C₉H₈BrNO₂
thermostat Physical Properties
Boiling Point 322.93°C
inventory_2 Storage & Handling
Density 1.521g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The presence of both the bromo and nitro functional groups makes it a valuable building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in drug discovery. Additionally, its structure allows for further modifications, enabling the creation of compounds with potential biological activity. It is also explored in material science for the synthesis of organic electronic materials due to its conjugated system.

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Test Parameter Specification
Appearance yellow powder
Purity 97-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,392.00
inventory 250mg
10-20 days ฿1,755.00

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(E)-1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene
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This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The presence of both the bromo and nitro functional groups makes it a valuable building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in drug discovery. Additionally, its structure allows for further modifications, enabling the creation of com
This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The presence of both the bromo and nitro functional groups makes it a valuable building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in drug discovery. Additionally, its structure allows for further modifications, enabling the creation of compounds with potential biological activity. It is also explored in material science for the synthesis of organic electronic materials due to its conjugated system.
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