(4-((Methylamino)methyl)phenyl)boronic acid

95%

Reagent Code: #203384
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CAS Number 518336-26-0

science Other reagents with same CAS 518336-26-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165 g/mol
Formula C₈H₁₂BNO₂
badge Registry Numbers
MDL Number MFCD03094948
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds. The methylamino group adds polarity and reactivity, useful in medicinal chemistry for designing bioactive molecules. Also employed in the synthesis of sensors and functional materials due to its ability to interact with diols and carbonyl compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,470.00
inventory 250mg
10-20 days ฿9,310.00
inventory 1g
10-20 days ฿24,200.00
(4-((Methylamino)methyl)phenyl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds. The methylamino group adds polarity and reactivity, useful in medicinal chemistry for designing bioactive molecules. Also employed in the synthesis of sensors and functional materials due to its ability to intera

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds. The methylamino group adds polarity and reactivity, useful in medicinal chemistry for designing bioactive molecules. Also employed in the synthesis of sensors and functional materials due to its ability to interact with diols and carbonyl compounds.

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