4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)morpholine

≥95%

Reagent Code: #118585
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CAS Number 364794-81-0

science Other reagents with same CAS 364794-81-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.23 g/mol
Formula C₁₈H₂₈BNO₃
badge Registry Numbers
MDL Number MFCD04440855
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds in pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive compounds and drug candidates due to its stability and reactivity under mild conditions. Its morpholine moiety further enhances its solubility and compatibility in various reaction environments, making it a versatile tool in medicinal chemistry and material science research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,339.00
inventory 100mg
10-20 days ฿1,971.00
inventory 1g
10-20 days ฿9,000.00

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4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)morpholine
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds in pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive compounds and drug candidates due to its stability and reactivity under mild c

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds in pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive compounds and drug candidates due to its stability and reactivity under mild conditions. Its morpholine moiety further enhances its solubility and compatibility in various reaction environments, making it a versatile tool in medicinal chemistry and material science research.

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