Methyl 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

97%

Reagent Code: #206770
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CAS Number 478375-39-2

science Other reagents with same CAS 478375-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.14 g/mol
Formula C₁₅H₂₁BO₄
thermostat Physical Properties
Boiling Point 370.4±35.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in cross-coupling reactions such as Suzuki-Miyaura coupling, this compound serves as a key building block in the synthesis of complex organic molecules. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. It is especially useful in medicinal chemistry for modifying aromatic cores to fine-tune biological activity. The methyl ester functionality allows further derivatization, such as hydrolysis to the corresponding carboxylic acid or conversion to amides, enabling diverse molecular design in drug discovery and materials science.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿720.00
5g
10-20 days ฿3,560.00
25g
10-20 days ฿17,810.00
Methyl 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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Used primarily in cross-coupling reactions such as Suzuki-Miyaura coupling, this compound serves as a key building block in the synthesis of complex organic molecules. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. It is especially useful in medicinal chemistry for modifying aromatic cores to fine-tune biological activity. The methyl ester functionality allows further derivatization,

Used primarily in cross-coupling reactions such as Suzuki-Miyaura coupling, this compound serves as a key building block in the synthesis of complex organic molecules. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. It is especially useful in medicinal chemistry for modifying aromatic cores to fine-tune biological activity. The methyl ester functionality allows further derivatization, such as hydrolysis to the corresponding carboxylic acid or conversion to amides, enabling diverse molecular design in drug discovery and materials science.

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