2-(2,6-Difluoro-3,5-dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Reagent Code: #41287
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CAS Number 1614233-69-0

science Other reagents with same CAS 1614233-69-0

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Weight 300.1061 g/mol
Formula C₁₄H₁₉BF₂O₄
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MDL Number MFCD30067285
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This compound is primarily utilized in organic synthesis as a versatile boron-containing reagent. It plays a crucial role in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is widely employed in the formation of carbon-carbon bonds. Its stability and reactivity make it a valuable intermediate in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of organic electronic materials due to its ability to facilitate the creation of conjugated systems. Its fluorine and methoxy substituents further enhance its utility in fine-tuning the electronic properties of target molecules.

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inventory 50mg
10-20 days ฿5,940.00

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2-(2,6-Difluoro-3,5-dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis as a versatile boron-containing reagent. It plays a crucial role in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is widely employed in the formation of carbon-carbon bonds. Its stability and reactivity make it a valuable intermediate in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of organic electronic materials due

This compound is primarily utilized in organic synthesis as a versatile boron-containing reagent. It plays a crucial role in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is widely employed in the formation of carbon-carbon bonds. Its stability and reactivity make it a valuable intermediate in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of organic electronic materials due to its ability to facilitate the creation of conjugated systems. Its fluorine and methoxy substituents further enhance its utility in fine-tuning the electronic properties of target molecules.

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