4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)thiomorpholine 1,1-dioxide

95%

Reagent Code: #118579
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CAS Number 1092563-25-1

science Other reagents with same CAS 1092563-25-1

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Weight 351.27 g/mol
Formula C₁₇H₂₆BNO₄S
badge Registry Numbers
MDL Number MFCD22056473
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas

description Product Description

Used in organic synthesis as a key intermediate for the preparation of boron-containing compounds, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the pharmaceutical industry to create complex molecules for drug development. It also serves as a building block in the synthesis of bioactive molecules and materials with potential applications in medicinal chemistry and material science. Its thiomorpholine 1,1-dioxide moiety can enhance the solubility and stability of the resulting compounds, making it valuable in designing drug candidates with improved pharmacokinetic properties. Additionally, it is utilized in the development of boron-based probes for imaging and diagnostic purposes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,974.00
inventory 1g
10-20 days ฿36,567.00
inventory 250mg
10-20 days ฿13,545.00

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4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)thiomorpholine 1,1-dioxide
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Used in organic synthesis as a key intermediate for the preparation of boron-containing compounds, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the pharmaceutical industry to create complex molecules for drug development. It also serves as a building block in the synthesis of bioactive molecules and materials with potential applications in medicinal chemistry and material science. Its thiomorpholine 1,1-dioxide moiety can enhance the solubility and stabi

Used in organic synthesis as a key intermediate for the preparation of boron-containing compounds, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the pharmaceutical industry to create complex molecules for drug development. It also serves as a building block in the synthesis of bioactive molecules and materials with potential applications in medicinal chemistry and material science. Its thiomorpholine 1,1-dioxide moiety can enhance the solubility and stability of the resulting compounds, making it valuable in designing drug candidates with improved pharmacokinetic properties. Additionally, it is utilized in the development of boron-based probes for imaging and diagnostic purposes.

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