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

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Reagent Code: #118380
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CAS Number 1005206-25-6

science Other reagents with same CAS 1005206-25-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.14 g/mol
Formula C₁₃H₁₆BF₃O₂S
badge Registry Numbers
MDL Number MFCD11042448
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boron reagent. Its structure, featuring a trifluoromethylthio group, makes it valuable for introducing this functional group into various organic compounds, which is beneficial in the development of pharmaceuticals and agrochemicals. The compound’s stability and reactivity also make it suitable for creating complex molecules in medicinal chemistry, especially in the synthesis of drug candidates with enhanced biological activity. Additionally, it is used in material science for modifying polymers and creating advanced materials with specific properties.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,583.00
inventory 100mg
10-20 days ฿1,521.00

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4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)thio)phenyl)-1,3,2-dioxaborolane
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boron reagent. Its structure, featuring a trifluoromethylthio group, makes it valuable for introducing this functional group into various organic compounds, which is beneficial in the development of pharmaceuticals and agrochemicals. The compound’s stability and reactivity also make it suitable for creating complex molecules in medicinal chemistry, especi

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boron reagent. Its structure, featuring a trifluoromethylthio group, makes it valuable for introducing this functional group into various organic compounds, which is beneficial in the development of pharmaceuticals and agrochemicals. The compound’s stability and reactivity also make it suitable for creating complex molecules in medicinal chemistry, especially in the synthesis of drug candidates with enhanced biological activity. Additionally, it is used in material science for modifying polymers and creating advanced materials with specific properties.

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