(4-(2-(1,4-Dioxa-8-azaspiro[4.5]decan-8- yl)ethoxy)-3-fluorophenyl)boronic acid

98%

Reagent Code: #89229
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CAS Number 1704082-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.14 g/mol
Formula C₁₅H₂₁BFNO₅
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables it to act as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the fluorophenyl moiety enhances its reactivity and selectivity in these reactions, making it valuable for constructing biologically active compounds. Additionally, the dioxa-azaspirodecane structure contributes to its stability and solubility, facilitating its use in various catalytic processes. It is often employed in research and development settings to explore new drug candidates or optimize existing therapeutic agents.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days €1,117.60
(4-(2-(1,4-Dioxa-8-azaspiro[4.5]decan-8- yl)ethoxy)-3-fluorophenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables it to act as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the fluorophenyl moiety enhances its reactivity and selectivity in these reactions, making it valuable for constructing biologically active compounds. Additionally, the dioxa-azaspirodecane structure contributes to its stability and solubility, facilitating its use in various catalytic processes. It is often employed in research and development settings to explore new drug candidates or optimize existing therapeutic agents.
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