2-Bromo-N-ethylbenzamide

95%

Reagent Code: #150895
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CAS Number 80031-02-3

science Other reagents with same CAS 80031-02-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.09 g/mol
Formula C₉H₁₀BrNO
badge Registry Numbers
MDL Number MFCD01211894
thermostat Physical Properties
Melting Point 91-95 °C
Boiling Point 330.5±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.403±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block for the preparation of more complex molecules due to the presence of both amide and bromo functional groups. The bromine atom allows for further transformations via cross-coupling reactions such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The compound is also utilized in the development of bioactive compounds, including potential medicinal agents targeting central nervous system disorders or inflammation. Its reactivity and structural features make it valuable in research settings for designing novel organic compounds.

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Test Parameter Specification
Appearance yellow solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,890.00
inventory 5g
10-20 days ฿6,030.00

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2-Bromo-N-ethylbenzamide
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block for the preparation of more complex molecules due to the presence of both amide and bromo functional groups. The bromine atom allows for further transformations via cross-coupling reactions such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The compound is also utilized in the development of bioactive compounds, including potential medicinal

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block for the preparation of more complex molecules due to the presence of both amide and bromo functional groups. The bromine atom allows for further transformations via cross-coupling reactions such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The compound is also utilized in the development of bioactive compounds, including potential medicinal agents targeting central nervous system disorders or inflammation. Its reactivity and structural features make it valuable in research settings for designing novel organic compounds.

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