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

95%

Reagent Code: #182605
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CAS Number 1198615-87-0

science Other reagents with same CAS 1198615-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.16 g/mol
Formula C₁₆H₂₃BO₄
badge Registry Numbers
MDL Number MFCD18383986
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the introduction of substituted aromatic systems. Its ester functionality provides a handle for further transformations, such as hydrolysis or reduction, making it valuable in multi-step synthetic routes. Commonly employed in medicinal chemistry for constructing biaryl scaffolds found in bioactive compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿810.00
inventory 1g
10-20 days ฿3,150.00
inventory 5g
10-20 days ฿15,320.00
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Ethyl 2-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the introduction of substituted aromatic systems. Its ester functionality provides a handle for further transformations, such as hydrolysis or reduction, making it valuable in multi-step synth

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the introduction of substituted aromatic systems. Its ester functionality provides a handle for further transformations, such as hydrolysis or reduction, making it valuable in multi-step synthetic routes. Commonly employed in medicinal chemistry for constructing biaryl scaffolds found in bioactive compounds.

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