5-bromo-3-methylisoquinoline

≥95%

Reagent Code: #143957
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CAS Number 16552-67-3

science Other reagents with same CAS 16552-67-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.08 g/mol
Formula C₁₀H₈BrN
badge Registry Numbers
MDL Number MFCD18260472
inventory_2 Storage & Handling
Density 1.488±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, 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. Its bromine functionality allows for selective functionalization via palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations. Also employed in research settings to design bioactive molecules targeting neurological disorders and inflammation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,410.00

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5-bromo-3-methylisoquinoline
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Used as a key intermediate in the synthesis of pharmaceuticals, 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. Its bromine functionality allows for selective functionalization via palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations. Also employed in research settings to design bioa

Used as a key intermediate in the synthesis of pharmaceuticals, 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. Its bromine functionality allows for selective functionalization via palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations. Also employed in research settings to design bioactive molecules targeting neurological disorders and inflammation.

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