4,4,5,5-Tetramethyl-2-(3-((2,2,2-trifluoroethyl)thio)phenyl)-1,3,2-dioxaborolane

97%

Reagent Code: #118373
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CAS Number 1026797-07-8

science Other reagents with same CAS 1026797-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.16 g/mol
Formula C₁₄H₁₈BF₃O₂S
badge Registry Numbers
MDL Number MFCD11520054
thermostat Physical Properties
Boiling Point 354.1±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling of aromatic rings is required. Additionally, it finds use in materials science for the development of organic electronic materials, where its stability and reactivity are advantageous. Its trifluoroethylthio group further enhances its utility in creating compounds with unique electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,816.00
inventory 5g
10-20 days ฿60,570.00
inventory 1g
10-20 days ฿20,556.00
inventory 250mg
10-20 days ฿7,605.00

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4,4,5,5-Tetramethyl-2-(3-((2,2,2-trifluoroethyl)thio)phenyl)-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling of aromatic rings is required. Additionally, it finds use in materials science for the developmen

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling of aromatic rings is required. Additionally, it finds use in materials science for the development of organic electronic materials, where its stability and reactivity are advantageous. Its trifluoroethylthio group further enhances its utility in creating compounds with unique electronic properties.

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