1,3-Dihydroisobenzofuran-5-boronic Acid Pinacol Ester

≥98%

Reagent Code: #179577
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CAS Number 1352037-60-5

science Other reagents with same CAS 1352037-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.11 g/mol
Formula C₁₄H₁₉O₃B
badge Registry Numbers
MDL Number MFCD22628089
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester functionality provides enhanced stability and reactivity, making it valuable for constructing biaryl compounds and complex organic molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) where precise molecular architecture is required. The pinacol protecting group facilitates handling and storage while maintaining high coupling efficiency under mild reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,800.00
inventory 250mg
10-20 days ฿17,260.00
inventory 500mg
10-20 days ฿32,750.00
inventory 1g
10-20 days ฿46,270.00

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1,3-Dihydroisobenzofuran-5-boronic Acid Pinacol Ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester functionality provides enhanced stability and reactivity, making it valuable for constructing biaryl compounds and complex organic molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) where precise molecular architecture is required. The pinacol protecting group facilitates handling and s

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester functionality provides enhanced stability and reactivity, making it valuable for constructing biaryl compounds and complex organic molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) where precise molecular architecture is required. The pinacol protecting group facilitates handling and storage while maintaining high coupling efficiency under mild reaction conditions.

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