5-Bromo-2-fluoro-4-methylbenzonitrile

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Reagent Code: #120113
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CAS Number 1269493-45-9

science Other reagents with same CAS 1269493-45-9

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scatter_plot Molecular Information
Weight 214.03 g/mol
Formula C₈H₅BrFN
badge Registry Numbers
MDL Number MFCD18452117
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique bromo and fluoro substituents make it particularly valuable in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig reactions, which are essential in pharmaceutical and agrochemical research. Additionally, the nitrile group in the molecule can be further transformed into other functional groups, enabling the synthesis of a wide range of derivatives. Its application is also seen in material science, where it contributes to the creation of advanced polymers and liquid crystals. Overall, its structural features make it a key building block in the design of molecules with potential biological and industrial significance.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿648.00
inventory 250mg
10-20 days ฿270.00
inventory 5g
10-20 days ฿2,457.00

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5-Bromo-2-fluoro-4-methylbenzonitrile
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This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique bromo and fluoro substituents make it particularly valuable in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig reactions, which are essential in pharmaceutical and agrochemical research. Additionally, the nitrile group in the molecule can be further transformed into other functional groups, enabling the synthes

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique bromo and fluoro substituents make it particularly valuable in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig reactions, which are essential in pharmaceutical and agrochemical research. Additionally, the nitrile group in the molecule can be further transformed into other functional groups, enabling the synthesis of a wide range of derivatives. Its application is also seen in material science, where it contributes to the creation of advanced polymers and liquid crystals. Overall, its structural features make it a key building block in the design of molecules with potential biological and industrial significance.

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