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

95%

Reagent Code: #130675
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CAS Number 887234-98-2

science Other reagents with same CAS 887234-98-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.14 g/mol
Formula C₁₅H₂₁BO₄
badge Registry Numbers
MDL Number MFCD16996352
thermostat Physical Properties
Boiling Point 385.4±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.07±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily in cross-coupling reactions, especially in Suzuki-Miyaura coupling, to construct biaryl and aryl-aryl systems in pharmaceutical and agrochemical synthesis. The boronate ester group acts as a key reactive handle, enabling efficient carbon-carbon bond formation under mild conditions. It is particularly valuable in late-stage functionalization of aromatic compounds due to its stability and selectivity. Commonly employed in the development of active pharmaceutical ingredients (APIs) and organic electronic materials where precise molecular architecture is required. Its methyl ester functionality allows for further derivatization, such as hydrolysis or reduction, expanding its utility in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,160.00
inventory 250mg
10-20 days ฿8,750.00
inventory 1g
10-20 days ฿23,610.00

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Methyl 3-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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Used primarily in cross-coupling reactions, especially in Suzuki-Miyaura coupling, to construct biaryl and aryl-aryl systems in pharmaceutical and agrochemical synthesis. The boronate ester group acts as a key reactive handle, enabling efficient carbon-carbon bond formation under mild conditions. It is particularly valuable in late-stage functionalization of aromatic compounds due to its stability and selectivity. Commonly employed in the development of active pharmaceutical ingredients (APIs) and organi

Used primarily in cross-coupling reactions, especially in Suzuki-Miyaura coupling, to construct biaryl and aryl-aryl systems in pharmaceutical and agrochemical synthesis. The boronate ester group acts as a key reactive handle, enabling efficient carbon-carbon bond formation under mild conditions. It is particularly valuable in late-stage functionalization of aromatic compounds due to its stability and selectivity. Commonly employed in the development of active pharmaceutical ingredients (APIs) and organic electronic materials where precise molecular architecture is required. Its methyl ester functionality allows for further derivatization, such as hydrolysis or reduction, expanding its utility in multi-step synthetic routes.

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