(4-Ethoxy-3-formylphenyl)boronic acid

98%

Reagent Code: #129199
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CAS Number 480424-63-3

science Other reagents with same CAS 480424-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.99 g/mol
Formula C₉H₁₁BO₄
badge Registry Numbers
MDL Number MFCD06801740
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. The aldehyde and boronic acid functional groups allow for sequential transformations, enabling the construction of complex aromatic structures. Commonly employed in the development of liquid crystals, dyes, and bioactive molecules due to its bifunctional reactivity. Also utilized in sensor design for detecting diols and carbohydrates through boronate ester formation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,070.00
inventory 1g
10-20 days ฿11,320.00

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(4-Ethoxy-3-formylphenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. The aldehyde and boronic acid functional groups allow for sequential transformations, enabling the construction of complex aromatic structures. Commonly employed in the development of liquid crystals, dyes, and bioactive molecules due to its bifunctional reactivity. Also utilized in sensor design for detecting diols and carbohydrates throug

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. The aldehyde and boronic acid functional groups allow for sequential transformations, enabling the construction of complex aromatic structures. Commonly employed in the development of liquid crystals, dyes, and bioactive molecules due to its bifunctional reactivity. Also utilized in sensor design for detecting diols and carbohydrates through boronate ester formation.

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