(2-Bromo-3-methylphenyl)boronic acid

98%

Reagent Code: #130979
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CAS Number 2304635-39-8

science Other reagents with same CAS 2304635-39-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.85 g/mol
Formula C₇H₈BBrO₂
badge Registry Numbers
MDL Number MFCD30834361
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, to construct biaryl compounds which are common scaffolds in pharmaceuticals and agrochemicals. Its boronic acid group enables carbon-carbon bond formation under mild conditions, making it valuable for building complex aromatic structures. Commonly employed in drug discovery and development for creating intermediates with specific substitution patterns on aromatic rings. Also utilized in materials science for synthesizing conjugated organic molecules used in electronic devices.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,220.00
inventory 5g
10-20 days ฿33,280.00
inventory 250mg
10-20 days ฿3,070.00

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(2-Bromo-3-methylphenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are common scaffolds in pharmaceuticals and agrochemicals. Its boronic acid group enables carbon-carbon bond formation under mild conditions, making it valuable for building complex aromatic structures. Commonly employed in drug discovery and development for creating intermediates with specific substitution patterns on aromatic rings. Also utilized in materials science for synthesizing

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are common scaffolds in pharmaceuticals and agrochemicals. Its boronic acid group enables carbon-carbon bond formation under mild conditions, making it valuable for building complex aromatic structures. Commonly employed in drug discovery and development for creating intermediates with specific substitution patterns on aromatic rings. Also utilized in materials science for synthesizing conjugated organic molecules used in electronic devices.

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