(4-(Benzyloxy)-2-formyl-5-methoxyphenyl)boronic acid

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Reagent Code: #113281
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CAS Number 1021431-39-9

science Other reagents with same CAS 1021431-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.09 g/mol
Formula C₁₅H₁₅BO₅
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MDL Number MFCD27976031
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules. This compound is also utilized in the development of sensors and probes for detecting specific analytes due to its boronic acid group, which can form reversible covalent bonds with diols and other functional groups. Additionally, it plays a role in the synthesis of materials for organic electronics and advanced polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,200.00
inventory 250mg
10-20 days ฿10,800.00
inventory 1g
10-20 days ฿26,973.00

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(4-(Benzyloxy)-2-formyl-5-methoxyphenyl)boronic acid
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Used in organic synthesis as a key intermediate for the preparation of various biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules. This compound is also utilized in the development of sensors and probes for detecting specific analytes due to its boronic acid group, which can form reversible covalent bonds with diols and other functional groups. Additionally, it plays a

Used in organic synthesis as a key intermediate for the preparation of various biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules. This compound is also utilized in the development of sensors and probes for detecting specific analytes due to its boronic acid group, which can form reversible covalent bonds with diols and other functional groups. Additionally, it plays a role in the synthesis of materials for organic electronics and advanced polymers.

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