2-Bromo-5-(trifluoromethoxy)benzaldehyde

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Reagent Code: #43270
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CAS Number 505084-61-7

science Other reagents with same CAS 505084-61-7

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Weight 269.0154 g/mol
Formula C₈H₄BrF₃O₂
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MDL Number MFCD07368722
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and trifluoromethoxy group, makes it valuable for constructing complex molecules, particularly in the development of active ingredients for drugs targeting neurological disorders and inflammation. Additionally, it is employed in the synthesis of advanced materials, including liquid crystals and polymers, where its unique electronic properties enhance performance. Its role in cross-coupling reactions further expands its application in creating specialized organic compounds for research and industrial purposes.

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inventory 250mg
10-20 days ฿3,339.00

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2-Bromo-5-(trifluoromethoxy)benzaldehyde
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and trifluoromethoxy group, makes it valuable for constructing complex molecules, particularly in the development of active ingredients for drugs targeting neurological disorders and inflammation. Additionally, it is employed in the synthesis of advanced materials, including liquid crystals and polymers, where its uniqu

This chemical is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and trifluoromethoxy group, makes it valuable for constructing complex molecules, particularly in the development of active ingredients for drugs targeting neurological disorders and inflammation. Additionally, it is employed in the synthesis of advanced materials, including liquid crystals and polymers, where its unique electronic properties enhance performance. Its role in cross-coupling reactions further expands its application in creating specialized organic compounds for research and industrial purposes.

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