3-Methylisoxazole-4-boronic Acid Pinacol Ester

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Reagent Code: #90242
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CAS Number 1421846-79-8

science Other reagents with same CAS 1421846-79-8

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Weight 209.05 g/mol
Formula C₁₀H₁₆NO₃B
badge Registry Numbers
MDL Number MFCD24040285
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This compound is particularly valuable in the development of biologically active molecules, including potential drug candidates. Its boronic ester group facilitates efficient and selective coupling with aryl or vinyl halides, making it a useful tool in medicinal chemistry and material science research. Additionally, it can be employed in the synthesis of complex organic compounds for use in electronic materials or as ligands in catalytic systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,420.00
inventory 1g
10-20 days ฿38,710.00

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3-Methylisoxazole-4-boronic Acid Pinacol Ester
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Used in organic synthesis as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This compound is particularly valuable in the development of biologically active molecules, including potential drug candidates. Its boronic ester group facilitates efficient and selective coupling with aryl or vinyl halides, making it a useful tool in medicinal ch

Used in organic synthesis as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This compound is particularly valuable in the development of biologically active molecules, including potential drug candidates. Its boronic ester group facilitates efficient and selective coupling with aryl or vinyl halides, making it a useful tool in medicinal chemistry and material science research. Additionally, it can be employed in the synthesis of complex organic compounds for use in electronic materials or as ligands in catalytic systems.

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