5-Chloro-2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

97%

Reagent Code: #48694
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CAS Number 1269232-96-3

science Other reagents with same CAS 1269232-96-3

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Weight 271.5234 g/mol
Formula C₁₂H₁₆BClFNO₂
badge Registry Numbers
MDL Number MFCD22189454
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description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules through cross-coupling reactions, such as Suzuki-Miyaura coupling, due to the presence of the boronate ester group. Its structure allows for selective functionalization, making it valuable in the synthesis of biologically active compounds. Additionally, it is employed in material science for the preparation of advanced organic materials, including polymers and small molecules with potential applications in electronics and optoelectronics. The chloro and fluoro substituents enhance its reactivity and stability, contributing to its versatility in various chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,958.00

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5-Chloro-2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules through cross-coupling reactions, such as Suzuki-Miyaura coupling, due to the presence of the boronate ester group. Its structure allows for selective functionalization, making it valuable in the synthesis of biologically active compounds. Additionally, it is employed in material science for th

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules through cross-coupling reactions, such as Suzuki-Miyaura coupling, due to the presence of the boronate ester group. Its structure allows for selective functionalization, making it valuable in the synthesis of biologically active compounds. Additionally, it is employed in material science for the preparation of advanced organic materials, including polymers and small molecules with potential applications in electronics and optoelectronics. The chloro and fluoro substituents enhance its reactivity and stability, contributing to its versatility in various chemical transformations.

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