5-Bromo-6-iodopyridin-2-amine

≥95%

Reagent Code: #120219
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CAS Number 1223748-35-3

science Other reagents with same CAS 1223748-35-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.91 g/mol
Formula C₅H₄BrIN₂
badge Registry Numbers
MDL Number MFCD14708215
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Used primarily as a building block in organic synthesis, this compound is valuable in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it a key intermediate in the creation of complex molecules. It is particularly useful in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to form carbon-carbon or carbon-nitrogen bonds. These reactions are essential in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it can serve as a precursor in the preparation of heterocyclic compounds, which are often explored for their therapeutic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,852.00
inventory 100mg
10-20 days ฿1,926.00
inventory 1g
10-20 days ฿9,576.00

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5-Bromo-6-iodopyridin-2-amine
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Used primarily as a building block in organic synthesis, this compound is valuable in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it a key intermediate in the creation of complex molecules. It is particularly useful in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to form carbon-carbon or carbon-nitrogen bonds. These reactions are essential in the synthesis of bioactive compounds, including potential drug candi

Used primarily as a building block in organic synthesis, this compound is valuable in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it a key intermediate in the creation of complex molecules. It is particularly useful in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to form carbon-carbon or carbon-nitrogen bonds. These reactions are essential in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it can serve as a precursor in the preparation of heterocyclic compounds, which are often explored for their therapeutic properties.

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