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

97%

Reagent Code: #119754
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CAS Number 741709-57-9

science Other reagents with same CAS 741709-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.12 g/mol
Formula C₁₄H₂₀BNO₄
badge Registry Numbers
MDL Number MFCD12923436
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Applied in the production of agrochemicals, aiding in the creation of novel pesticides and herbicides. Utilized in material science for the development of organic electronic materials, such as OLEDs and semiconductors. Also employed in research laboratories for the preparation of boron-containing compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿23,760.00
inventory 1g
10-20 days ฿5,319.00
inventory 250mg
10-20 days ฿2,016.00
inventory 100mg
10-20 days ฿1,053.00

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Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Applied in the production of agrochemicals, aiding in the creation of novel pesticides and herbicides. Utilized in material science for the development of organic electronic materials, such as OLEDs and semiconductors. Also emplo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Applied in the production of agrochemicals, aiding in the creation of novel pesticides and herbicides. Utilized in material science for the development of organic electronic materials, such as OLEDs and semiconductors. Also employed in research laboratories for the preparation of boron-containing compounds with potential biological activity.

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