Potassium trifluoro(thiomorpholinomethyl)borate

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Reagent Code: #46764
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CAS Number 1150654-80-0

science Other reagents with same CAS 1150654-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.11 g/mol
Formula C₅H₁₀BF₃KNS
badge Registry Numbers
MDL Number MFCD10700162
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized as a reagent in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it acts as a stable and easy-to-handle source of the trifluoro(thiomorpholinomethyl)borate anion. This enables efficient transfer of the thiomorpholinomethyl group to form new carbon-carbon bonds, facilitating the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the thiomorpholine moiety can impart unique reactivity or selectivity in certain transformations, enhancing its utility in targeted synthetic pathways.

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Test Parameter Specification
Appearance solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,734.00
inventory 5g
10-20 days ฿44,622.00
inventory 250mg
10-20 days ฿6,822.00

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Potassium trifluoro(thiomorpholinomethyl)borate
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This chemical is primarily utilized as a reagent in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it acts as a stable and easy-to-handle source of the trifluoro(thiomorpholinomethyl)borate anion. This enables efficient transfer of the thiomorpholinomethyl group to form new carbon-carbon bonds, facilitating the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the thiomorpholine moiety can impart unique reactivity or selectivity in ce

This chemical is primarily utilized as a reagent in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it acts as a stable and easy-to-handle source of the trifluoro(thiomorpholinomethyl)borate anion. This enables efficient transfer of the thiomorpholinomethyl group to form new carbon-carbon bonds, facilitating the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the thiomorpholine moiety can impart unique reactivity or selectivity in certain transformations, enhancing its utility in targeted synthetic pathways.

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