6-Bromo-2-methoxypyridin-3-ol

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Reagent Code: #49881
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CAS Number 1823333-27-2

science Other reagents with same CAS 1823333-27-2

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Weight 204.0213 g/mol
Formula C₆H₆BrNO₂
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MDL Number MFCD26517019
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6-Bromo-2-methoxypyridin-3-ol is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. It is often employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs), particularly in the creation of compounds with potential therapeutic properties. Additionally, it serves as a key building block in the production of agrochemicals, contributing to the development of pesticides and herbicides. Its reactivity and functional groups make it valuable in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,269.00
inventory 250mg
10-20 days ฿1,120.00
inventory 1g
10-20 days ฿4,490.00
inventory 5g
10-20 days ฿22,440.00

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6-Bromo-2-methoxypyridin-3-ol
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6-Bromo-2-methoxypyridin-3-ol is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. It is often employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs), particularly in the creation of compounds with potential therapeutic properties. Additionally, it serves as a key building block in the production of agrochemicals, contributing to the development of pesticides and herbicides. Its react

6-Bromo-2-methoxypyridin-3-ol is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. It is often employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs), particularly in the creation of compounds with potential therapeutic properties. Additionally, it serves as a key building block in the production of agrochemicals, contributing to the development of pesticides and herbicides. Its reactivity and functional groups make it valuable in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in medicinal chemistry and material science.

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