4-(Bromomethyl)-3,5-difluorobenzonitrile

95%

Reagent Code: #46566
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CAS Number 1239964-16-9

science Other reagents with same CAS 1239964-16-9

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Weight 232.0249 g/mol
Formula C₈H₄BrF₂N
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MDL Number MFCD21340277
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This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its functional groups, including the bromomethyl and nitrile moieties, make it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce fluorinated aromatic structures into target compounds. Additionally, the presence of fluorine atoms enhances the biological activity and metabolic stability of the resulting products, making it particularly useful in drug discovery and development. Its reactivity also allows for further modifications, enabling the synthesis of diverse derivatives for research and industrial applications.

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inventory 100mg
10-20 days ฿5,860.00

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4-(Bromomethyl)-3,5-difluorobenzonitrile
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This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its functional groups, including the bromomethyl and nitrile moieties, make it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce fluorinated aromatic structures into target compounds. Additionally, the presence of fluorine atoms enhances the b

This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its functional groups, including the bromomethyl and nitrile moieties, make it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce fluorinated aromatic structures into target compounds. Additionally, the presence of fluorine atoms enhances the biological activity and metabolic stability of the resulting products, making it particularly useful in drug discovery and development. Its reactivity also allows for further modifications, enabling the synthesis of diverse derivatives for research and industrial applications.

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