3-Hexamethyleneoxide boronic acid

95%

Reagent Code: #90079
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CAS Number 2225153-13-7

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.79436 g/mol
Formula C₆H₁₄B₂O₅
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various boron-containing compounds. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group is particularly valuable in creating complex molecular structures with high precision. Additionally, it is employed in the development of sensors and probes for detecting biological molecules due to its ability to interact with diols and other functional groups.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿49,600.00
100mg
10-20 days ฿148,800.00
3-Hexamethyleneoxide boronic acid
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Used in organic synthesis as a key intermediate for the preparation of various boron-containing compounds. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group is particularly valuable in creating complex molecular structures with high precision. Additionally, it is employed in the development of sensors and probes for detecting biological mol

Used in organic synthesis as a key intermediate for the preparation of various boron-containing compounds. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group is particularly valuable in creating complex molecular structures with high precision. Additionally, it is employed in the development of sensors and probes for detecting biological molecules due to its ability to interact with diols and other functional groups.

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