ethyl 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzoate

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Reagent Code: #183483
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CAS Number 346656-34-6

science Other reagents with same CAS 346656-34-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.1093 g/mol
Formula C₁₄H₁₉BO₄
badge Registry Numbers
MDL Number MFCD00064090
thermostat Physical Properties
Boiling Point 384.8℃ at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8℃, dry, sealed

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable for constructing biaryl frameworks found in active pharmaceutical ingredients. The presence of the ester group allows for further functionalization, such as hydrolysis or reduction, adding versatility in synthetic pathways. Stable and compatible with a range of reaction conditions, it is particularly useful in late-stage functionalization during drug development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿478.50
inventory 1g
10-20 days ฿1,034.00
inventory 5g
10-20 days ฿4,312.00

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ethyl 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzoate
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable for constructing biaryl frameworks found in active pharmaceutical ingredients. The presence of the ester group allows for further functionalization, such as hydrolysis or reduction, adding versatility in synthetic pathways. Stable and compatible w

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable for constructing biaryl frameworks found in active pharmaceutical ingredients. The presence of the ester group allows for further functionalization, such as hydrolysis or reduction, adding versatility in synthetic pathways. Stable and compatible with a range of reaction conditions, it is particularly useful in late-stage functionalization during drug development.

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