5-Bromo-N-methylnicotinamide

97%

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.

Available Sizes & Pricing

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