4-Bromo-N-isopropylbenzamide

98%

Reagent Code: #47547
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CAS Number 336182-29-7

science Other reagents with same CAS 336182-29-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.1100 g/mol
Formula C₁₀H₁₂BrNO
badge Registry Numbers
MDL Number MFCD00465197
thermostat Physical Properties
Boiling Point 344.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.349g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. It serves as a key building block in the development of compounds with potential biological activities, such as inhibitors or modulators of specific enzymes or receptors. Additionally, it is employed in research settings for the study of structure-activity relationships in drug discovery. Its bromine atom makes it a versatile candidate for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of more complex molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,448.00

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4-Bromo-N-isopropylbenzamide
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This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. It serves as a key building block in the development of compounds with potential biological activities, such as inhibitors or modulators of specific enzymes or receptors. Additionally, it is employed in research settings for the study of structure-activity relationships in drug discovery. Its bromine atom makes it a versatile candidate for further functionalization

This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. It serves as a key building block in the development of compounds with potential biological activities, such as inhibitors or modulators of specific enzymes or receptors. Additionally, it is employed in research settings for the study of structure-activity relationships in drug discovery. Its bromine atom makes it a versatile candidate for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of more complex molecules.

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