4-Bromo-N-((tetrahydrofuran-2-yl)methyl)benzamide

98%

Reagent Code: #245669
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CAS Number 326898-76-4

science Other reagents with same CAS 326898-76-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.15 g/mol
Formula C₁₂H₁₄BrNO₂
thermostat Physical Properties
Boiling Point 429.7±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.408±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for constructing more complex molecules due to the presence of both bromine and amide 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 amide group provides polarity and can participate in hydrogen bonding, which is beneficial in drug design for improving target binding. Commonly employed in medicinal chemistry for synthesizing potential bioactive agents, including CNS modulators and anti-inflammatory candidates. Also utilized in research settings to prepare labeled compounds or probes for biochemical studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,990.00
inventory 5mg
10-20 days ฿4,390.00
inventory 25mg
10-20 days ฿8,790.00

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4-Bromo-N-((tetrahydrofuran-2-yl)methyl)benzamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for constructing more complex molecules due to the presence of both bromine and amide 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 amide group provides polarity and can participate in hydrogen bonding, which is beneficial in drug de

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for constructing more complex molecules due to the presence of both bromine and amide 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 amide group provides polarity and can participate in hydrogen bonding, which is beneficial in drug design for improving target binding. Commonly employed in medicinal chemistry for synthesizing potential bioactive agents, including CNS modulators and anti-inflammatory candidates. Also utilized in research settings to prepare labeled compounds or probes for biochemical studies.

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