(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(thiomorpholino)methanone

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Reagent Code: #129801
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CAS Number 1509931-83-2

science Other reagents with same CAS 1509931-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.25 g/mol
Formula C₁₇H₂₄BNO₃S
badge Registry Numbers
MDL Number MFCD28167020
thermostat Physical Properties
Boiling Point 502.9±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in pharmaceutical synthesis, this compound plays a key role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronate ester group facilitates coupling with aryl halides, making it valuable in the development of bioactive compounds and drug candidates. The thiomorpholine moiety contributes to solubility and binding properties, which is advantageous in medicinal chemistry for optimizing pharmacokinetics. It is particularly useful in the synthesis of kinase inhibitors and other targeted therapies in oncology research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,960.00
inventory 250mg
10-20 days ฿3,320.00

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(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(thiomorpholino)methanone
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Used primarily as an intermediate in pharmaceutical synthesis, this compound plays a key role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronate ester group facilitates coupling with aryl halides, making it valuable in the development of bioactive compounds and drug candidates. The thiomorpholine moiety contributes to solubility and binding properties, which is advantageous in medicinal chemistry for optimizing pharmacokine

Used primarily as an intermediate in pharmaceutical synthesis, this compound plays a key role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronate ester group facilitates coupling with aryl halides, making it valuable in the development of bioactive compounds and drug candidates. The thiomorpholine moiety contributes to solubility and binding properties, which is advantageous in medicinal chemistry for optimizing pharmacokinetics. It is particularly useful in the synthesis of kinase inhibitors and other targeted therapies in oncology research.

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