Lithium triisopropoxy(4-(trifluoromethyl)pyridin-2-yl)borate

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Reagent Code: #130981
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CAS Number 2095458-45-8

science Other reagents with same CAS 2095458-45-8

blur_circular Chemical Specifications

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Weight 341.1 g/mol
Formula C₁₅H₂₄BF₃LiNO₃
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Lithium triisopropoxy(4-(trifluoromethyl)pyridin-2-yl)borate is an organoborate reagent used in advanced organic synthesis, particularly as a nucleophilic boron source in cross-coupling reactions such as the Suzuki-Miyaura coupling. It facilitates the introduction of the 4-(trifluoromethyl)pyridin-2-yl moiety into aryl and heteroaryl frameworks, forming carbon-carbon bonds essential for constructing complex molecules. Compared to other borates, it exhibits enhanced stability to air and moisture, simplifying laboratory handling. This reagent enables efficient reactions under mild conditions, improving yields and reducing byproducts. It is particularly valuable in the production of pharmaceuticals, agrochemicals, and specialty materials requiring heterocyclic components.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,990.00
inventory 250mg
10-20 days ฿4,060.00

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Lithium triisopropoxy(4-(trifluoromethyl)pyridin-2-yl)borate
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Lithium triisopropoxy(4-(trifluoromethyl)pyridin-2-yl)borate is an organoborate reagent used in advanced organic synthesis, particularly as a nucleophilic boron source in cross-coupling reactions such as the Suzuki-Miyaura coupling. It facilitates the introduction of the 4-(trifluoromethyl)pyridin-2-yl moiety into aryl and heteroaryl frameworks, forming carbon-carbon bonds essential for constructing complex molecules. Compared to other borates, it exhibits enhanced stability to air and moisture, simplify

Lithium triisopropoxy(4-(trifluoromethyl)pyridin-2-yl)borate is an organoborate reagent used in advanced organic synthesis, particularly as a nucleophilic boron source in cross-coupling reactions such as the Suzuki-Miyaura coupling. It facilitates the introduction of the 4-(trifluoromethyl)pyridin-2-yl moiety into aryl and heteroaryl frameworks, forming carbon-carbon bonds essential for constructing complex molecules. Compared to other borates, it exhibits enhanced stability to air and moisture, simplifying laboratory handling. This reagent enables efficient reactions under mild conditions, improving yields and reducing byproducts. It is particularly valuable in the production of pharmaceuticals, agrochemicals, and specialty materials requiring heterocyclic components.

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