3-Methoxy-4-carboxyphenylboronic acid

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Reagent Code: #90249
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CAS Number 851335-12-1

science Other reagents with same CAS 851335-12-1

blur_circular Chemical Specifications

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Weight 195.97 g/mol
Formula C₈H₉BO₅
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MDL Number MFCD06656278
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key building block for creating complex organic molecules, especially in the pharmaceutical industry for drug development. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl compounds. Additionally, it is utilized in material science for designing advanced polymers and sensors. Its methoxy and carboxyl groups further enhance its reactivity and versatility in various chemical transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,863.00
inventory 5g
10-20 days ฿8,946.00

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3-Methoxy-4-carboxyphenylboronic acid
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key building block for creating complex organic molecules, especially in the pharmaceutical industry for drug development. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl compounds. Additionally, it is utilized in material science for designing advanced polymers and sensors. Its methoxy and carboxyl groups further enhance

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key building block for creating complex organic molecules, especially in the pharmaceutical industry for drug development. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl compounds. Additionally, it is utilized in material science for designing advanced polymers and sensors. Its methoxy and carboxyl groups further enhance its reactivity and versatility in various chemical transformations.

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