2-(trifluoromethyl)-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

≥95%

Reagent Code: #240256
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CAS Number 1612287-99-6

science Other reagents with same CAS 1612287-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.09 g/mol
Formula C₁₃H₁₇BF₃NO₂
badge Registry Numbers
MDL Number MFCD18726737
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation, particularly in the development of trifluoromethyl-substituted heteroaromatic compounds, which are valuable in drug discovery due to enhanced metabolic stability and bioavailability. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds found in bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,440.00
inventory 250mg
10-20 days ฿12,930.00

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2-(trifluoromethyl)-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation, particularly in the development of trifluoromethyl-substituted heteroaromatic compounds, which are valuable in drug discovery due to enhanced metabolic stability and bioavailability. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds found in bioactive molecules.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation, particularly in the development of trifluoromethyl-substituted heteroaromatic compounds, which are valuable in drug discovery due to enhanced metabolic stability and bioavailability. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds found in bioactive molecules.

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