N-(4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)cyclohexanamine

98%

Reagent Code: #215908
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CAS Number 1256360-60-7

science Other reagents with same CAS 1256360-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.25 g/mol
Formula C₁₉H₂₉BFNO₂
badge Registry Numbers
MDL Number MFCD18087742
thermostat Physical Properties
Boiling Point 439.5±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.06±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceutical compounds. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in drug discovery and development. Commonly applied in the preparation of bioactive molecules and functionalized amines for medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,240.00
inventory 1g
10-20 days ฿11,290.00
inventory 5g
10-20 days ฿42,770.00

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N-(4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)cyclohexanamine
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Used as an intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceutical compounds. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in drug discovery and development. Commonly applied in the preparation of bioactive molecules and functionalized amines for medicinal chemistry research.

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceutical compounds. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in drug discovery and development. Commonly applied in the preparation of bioactive molecules and functionalized amines for medicinal chemistry research.

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