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

≥95%

Reagent Code: #118477
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CAS Number 1206594-08-2

science Other reagents with same CAS 1206594-08-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.24 g/mol
Formula C₁₉H₂₈BNO₃
badge Registry Numbers
MDL Number MFCD22573395
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, its morpholine moiety can enhance solubility and bioavailability, making it valuable in designing drug candidates. The cyclopropyl group adds structural diversity, potentially contributing to the compound’s biological activity or stability in various applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,938.00
inventory 250mg
10-20 days ฿13,230.00
inventory 1g
10-20 days ฿37,359.00

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4-(1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)morpholine
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, its morpholine moiety can enhance solubility and bioavailability, making it valuable in de

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, its morpholine moiety can enhance solubility and bioavailability, making it valuable in designing drug candidates. The cyclopropyl group adds structural diversity, potentially contributing to the compound’s biological activity or stability in various applications.

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