2-(Benzyloxy)-5-bromo-3-methoxypyridine

95%

Reagent Code: #151504
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CAS Number 1887247-39-3

science Other reagents with same CAS 1887247-39-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.15 g/mol
Formula C₁₃H₁₂BrNO₂
badge Registry Numbers
MDL Number MFCD30834030
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in medicinal chemistry research. Also utilized in the preparation of serotonin receptor modulators and antitumor agents. Preferred in late-stage derivatization due to the stability and reactivity of the bromine and ether functionalities.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿19,830.00
inventory 1g
10-20 days ฿26,420.00

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2-(Benzyloxy)-5-bromo-3-methoxypyridine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in medicinal chemistry research. Also utilized in the preparation of serotonin receptor modulators and

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in medicinal chemistry research. Also utilized in the preparation of serotonin receptor modulators and antitumor agents. Preferred in late-stage derivatization due to the stability and reactivity of the bromine and ether functionalities.

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