4-Bromo-N-phenylbenzamide

98%

Reagent Code: #147105
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CAS Number 6846-12-4

science Other reagents with same CAS 6846-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.13 g/mol
Formula C₁₃H₁₀BrNO
badge Registry Numbers
MDL Number MFCD00624477
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of biaryl compounds and other complex aromatic structures. Its bromine functionality allows for selective functionalization, making it valuable in medicinal chemistry for designing drug candidates with specific biological activity. Also employed in the synthesis of liquid crystals and organic electronic materials due to its stable aromatic framework and derivatization potential.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,730.00
inventory 1g
10-20 days ฿6,222.00

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4-Bromo-N-phenylbenzamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of biaryl compounds and other complex aromatic structures. Its bromine functionality allows for selective functionalization, making it valuable in medicinal chemistry for designing drug candidates with specific biological activity. Also employed in the synthesis of liquid cry

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of biaryl compounds and other complex aromatic structures. Its bromine functionality allows for selective functionalization, making it valuable in medicinal chemistry for designing drug candidates with specific biological activity. Also employed in the synthesis of liquid crystals and organic electronic materials due to its stable aromatic framework and derivatization potential.

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