(4-(3-Methylureido)phenyl)boronic acid

95%

Reagent Code: #131631
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CAS Number 1182315-47-4

science Other reagents with same CAS 1182315-47-4

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scatter_plot Molecular Information
Weight 194 g/mol
Formula C₈H₁₁BN₂O₃
badge Registry Numbers
MDL Number MFCD24615150
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid group facilitates coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research. The presence of a methylureido group provides hydrogen bonding capability, useful in designing enzyme inhibitors or receptor ligands. Also employed in the development of sensors and functional materials due to its selective binding properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,900.00
inventory 250mg
10-20 days ฿4,930.00
inventory 1g
10-20 days ฿13,300.00

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(4-(3-Methylureido)phenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid group facilitates coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research. The presence of a methylureido group provides hydrogen bonding capability, useful in designing enzyme inhibitors or receptor ligands. Also employed in the development of sensors and functional materials due to its select
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid group facilitates coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research. The presence of a methylureido group provides hydrogen bonding capability, useful in designing enzyme inhibitors or receptor ligands. Also employed in the development of sensors and functional materials due to its selective binding properties.
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