N-(5-Bromopyridin-2-yl)butyramide

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Reagent Code: #219472
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CAS Number 148612-12-8

science Other reagents with same CAS 148612-12-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.10 g/mol
Formula C₉H₁₁BrN₂O
badge Registry Numbers
MDL Number MFCD02210530
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to participate in cross-coupling reactions, enabling the construction of complex heterocyclic systems. Also employed in agrochemical research for designing bioactive molecules with potential pesticidal or herbicidal activity. Its bromine functionality allows for further functionalization via palladium-catalyzed reactions, making it valuable in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿990.00
inventory 250mg
10-20 days ฿2,190.00
inventory 1g
10-20 days ฿6,990.00

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N-(5-Bromopyridin-2-yl)butyramide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to participate in cross-coupling reactions, enabling the construction of complex heterocyclic systems. Also employed in agrochemical research for designing bioactive molecules with potential pesticidal or herbicidal activity. Its bromine functionality allows for further functionalization via

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to participate in cross-coupling reactions, enabling the construction of complex heterocyclic systems. Also employed in agrochemical research for designing bioactive molecules with potential pesticidal or herbicidal activity. Its bromine functionality allows for further functionalization via palladium-catalyzed reactions, making it valuable in structure-activity relationship studies.

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