N-benzyl 2-bromobenzamide

95%

Reagent Code: #126398
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CAS Number 82082-50-6

science Other reagents with same CAS 82082-50-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.16 g/mol
Formula C14H12BrNO
badge Registry Numbers
MDL Number MFCD00227668
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The presence of both the benzyl and bromo groups makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential for creating carbon-carbon and carbon-nitrogen bonds. Additionally, it serves as a key building block in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Its role in facilitating the introduction of aromatic and heteroaromatic structures into molecules makes it a crucial component in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿3,700.00
inventory 5g
10-20 days ฿14,800.00
inventory 25g
10-20 days ฿66,600.00

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N-benzyl 2-bromobenzamide
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This compound is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The presence of both the benzyl and bromo groups makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential for creating carbon-carbon and carbon-nitrogen bonds. Additionally, it serves as a key building block in the synthe

This compound is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The presence of both the benzyl and bromo groups makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential for creating carbon-carbon and carbon-nitrogen bonds. Additionally, it serves as a key building block in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Its role in facilitating the introduction of aromatic and heteroaromatic structures into molecules makes it a crucial component in medicinal chemistry research.

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