2-(Methylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile

≥95%

Reagent Code: #80777
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CAS Number 1346809-48-0

science Other reagents with same CAS 1346809-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.11 g/mol
Formula C₁₃H₁₈BN₃O₂
badge Registry Numbers
MDL Number MFCD16995277
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Additionally, it is employed in material science for creating advanced polymers and organic electronic materials. Its nitrile group further enhances its reactivity, enabling diverse chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,476.00
inventory 250mg
10-20 days ฿20,952.00

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2-(Methylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Additionally, it is employed in material science for creating advanced polymers and organic electronic materials. Its nitrile group further enhances its reactivity, enabling div

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Additionally, it is employed in material science for creating advanced polymers and organic electronic materials. Its nitrile group further enhances its reactivity, enabling diverse chemical transformations.

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