5-Bromo-2-(dimethylamino)pyridine

98%

Reagent Code: #144496
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CAS Number 26163-07-5

science Other reagents with same CAS 26163-07-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.06 g/mol
Formula C₇H₉BrN₂
badge Registry Numbers
MDL Number MFCD00099486
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients. Its bromine moiety facilitates metal-catalyzed transformations, enhancing its utility in late-stage diversification during drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿420.00
inventory 5g
10-20 days ฿1,920.00

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5-Bromo-2-(dimethylamino)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients. Its

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients. Its bromine moiety facilitates metal-catalyzed transformations, enhancing its utility in late-stage diversification during drug discovery.

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