4-Fluoro-2-(methoxymethyl)phenylboronic acid

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Reagent Code: #90590
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CAS Number 946607-86-9

science Other reagents with same CAS 946607-86-9

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Weight 183.98 g/mol
Formula C₈H₁₀BFO₃
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MDL Number MFCD28009343
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used primarily in organic synthesis, this compound acts as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. It is particularly valuable in the pharmaceutical industry for constructing complex molecules, including drug candidates. Its boronic acid group facilitates the coupling with aryl halides, making it essential for producing biaryl compounds. The 4-fluoro substituent introduces specific electronic effects, while the 2-methoxymethyl group enhances stability and reactivity. Additionally, it finds applications in material science for developing advanced polymers and electronic materials, as well as in agrochemical synthesis.

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inventory 1g
10-20 days ฿35,150.00

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4-Fluoro-2-(methoxymethyl)phenylboronic acid
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Used primarily in organic synthesis, this compound acts as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. It is particularly valuable in the pharmaceutical industry for constructing complex molecules, including drug candidates. Its boronic acid group facilitates the coupling with aryl halides, making it essential for producing biaryl compounds. The 4-fluoro substituent introduces specific electronic effects, while the 2-methoxymethyl group en

Used primarily in organic synthesis, this compound acts as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. It is particularly valuable in the pharmaceutical industry for constructing complex molecules, including drug candidates. Its boronic acid group facilitates the coupling with aryl halides, making it essential for producing biaryl compounds. The 4-fluoro substituent introduces specific electronic effects, while the 2-methoxymethyl group enhances stability and reactivity. Additionally, it finds applications in material science for developing advanced polymers and electronic materials, as well as in agrochemical synthesis.

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