5-Bromo-N-methylnicotinamide

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Reagent Code: #151069
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CAS Number 153435-68-8

science Other reagents with same CAS 153435-68-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.05 g/mol
Formula C₇H₇BrN₂O
badge Registry Numbers
MDL Number MFCD01788369
thermostat Physical Properties
Boiling Point 334.5±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.545±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the development of nicotinamide-based derivatives with potential therapeutic effects. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies, particularly in kinase inhibitors and enzyme modulators. Its bromine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification in drug discovery programs. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,510.00
inventory 5g
10-20 days ฿6,520.00
inventory 10g
10-20 days ฿12,000.00
inventory 25g
10-20 days ฿24,120.00

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5-Bromo-N-methylnicotinamide
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Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the development of nicotinamide-based derivatives with potential therapeutic effects. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies, particularly in kinase inhibitors and enzyme modulators. Its bromine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the development of nicotinamide-based derivatives with potential therapeutic effects. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies, particularly in kinase inhibitors and enzyme modulators. Its bromine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification in drug discovery programs. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.

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