4-Bromo-N-(tert-butyl)benzamide

97%

Reagent Code: #150218
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CAS Number 42498-38-4

science Other reagents with same CAS 42498-38-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.14 g/mol
Formula C₁₁H₁₄BrNO
badge Registry Numbers
MDL Number MFCD00462539
thermostat Physical Properties
Melting Point 134.98 °C
Boiling Point 350.5 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.309±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for selective bromination and coupling reactions, making it valuable in constructing complex molecules. Commonly employed in Suzuki and other palladium-catalyzed cross-coupling reactions to form biaryl systems. Also utilized in the synthesis of bioactive compounds where the tert-butyl group enhances metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿980.00
inventory 5g
10-20 days ฿4,760.00
inventory 25g
10-20 days ฿20,580.00

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4-Bromo-N-(tert-butyl)benzamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for selective bromination and coupling reactions, making it valuable in constructing complex molecules. Commonly employed in Suzuki and other palladium-catalyzed cross-coupling reactions to form biaryl systems. Also utilized in the synthesis of bioactive compounds where the tert-butyl group enhances metabolic stability.

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for selective bromination and coupling reactions, making it valuable in constructing complex molecules. Commonly employed in Suzuki and other palladium-catalyzed cross-coupling reactions to form biaryl systems. Also utilized in the synthesis of bioactive compounds where the tert-butyl group enhances metabolic stability.

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