5-Bromo-3-fluoro-2-(trifluoromethoxy)pyridine

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Reagent Code: #48969
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CAS Number 1361893-62-0

science Other reagents with same CAS 1361893-62-0

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Weight 259.9838 g/mol
Formula C₆H₂BrF₄NO
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MDL Number MFCD25451808
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Used primarily in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of active compounds. Its unique structure, featuring bromine and fluorine substituents, enhances reactivity and stability, making it valuable for developing new drugs and pesticides. In pharmaceuticals, it contributes to the creation of molecules with potential therapeutic effects, such as anti-inflammatory or antiviral properties. In agrochemicals, it aids in the design of pesticides with improved efficacy and selectivity. Additionally, its trifluoromethoxy group is particularly useful in modifying the physical and chemical properties of target molecules, enhancing their bioavailability and resistance to degradation.

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inventory 25mg
10-20 days ฿10,062.00

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5-Bromo-3-fluoro-2-(trifluoromethoxy)pyridine
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Used primarily in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of active compounds. Its unique structure, featuring bromine and fluorine substituents, enhances reactivity and stability, making it valuable for developing new drugs and pesticides. In pharmaceuticals, it contributes to the creation of molecules with potential therapeutic effects, such as anti-inflammatory or antiviral properties. In agrochemicals, it aids in the design of pesticides with improved eff

Used primarily in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of active compounds. Its unique structure, featuring bromine and fluorine substituents, enhances reactivity and stability, making it valuable for developing new drugs and pesticides. In pharmaceuticals, it contributes to the creation of molecules with potential therapeutic effects, such as anti-inflammatory or antiviral properties. In agrochemicals, it aids in the design of pesticides with improved efficacy and selectivity. Additionally, its trifluoromethoxy group is particularly useful in modifying the physical and chemical properties of target molecules, enhancing their bioavailability and resistance to degradation.

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