4-Bromo-N-methoxy-N-methylbenzamide

98%

Reagent Code: #145503
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CAS Number 192436-83-2

science Other reagents with same CAS 192436-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD02684303
thermostat Physical Properties
Boiling Point 351.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block in the preparation of bioactive molecules due to the presence of the bromo substituent, which allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. The N-methoxy-N-methyl amide group enhances stability and can act as a directing group in metal-catalyzed C–H activation processes. Commonly employed in the development of drug candidates where aromatic scaffolds are required for target binding. Also utilized in research settings for the synthesis of complex molecules requiring selective transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,170.00
inventory 10g
10-20 days ฿2,340.00
inventory 25g
10-20 days ฿5,220.00
inventory 100g
10-20 days ฿23,200.00

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4-Bromo-N-methoxy-N-methylbenzamide
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block in the preparation of bioactive molecules due to the presence of the bromo substituent, which allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. The N-methoxy-N-methyl amide group enhances stability and can act as a directing group in metal-catalyzed C–H activation processes. Commonly employed in the development of drug ca

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block in the preparation of bioactive molecules due to the presence of the bromo substituent, which allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. The N-methoxy-N-methyl amide group enhances stability and can act as a directing group in metal-catalyzed C–H activation processes. Commonly employed in the development of drug candidates where aromatic scaffolds are required for target binding. Also utilized in research settings for the synthesis of complex molecules requiring selective transformations.

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