Sodium 3,3,3-trifluoropropane-1-sulfinate

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Reagent Code: #236584
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CAS Number 1263377-91-8

science Other reagents with same CAS 1263377-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.11 g/mol
Formula C₃H₄F₃NaO₂S
badge Registry Numbers
MDL Number MFCD18379709
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key reagent in organic synthesis, particularly in 3,3,3-trifluoropropylation reactions. It serves as a source of the 3,3,3-trifluoropropyl (CF3CH2CH2-) group, enabling the introduction of fluorinated alkyl moieties into pharmaceuticals, agrochemicals, and functional materials. Its stability and reactivity under mild conditions make it suitable for late-stage functionalization in drug development. Commonly applied in transition-metal-catalyzed reactions, such as copper-catalyzed couplings with aryl halides, and radical processes to enhance metabolic stability, lipophilicity, and other physicochemical properties of target molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,890.00
inventory 250mg
10-20 days ฿4,230.00
inventory 1g
10-20 days ฿16,850.00
inventory 5g
10-20 days ฿73,130.00

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Sodium 3,3,3-trifluoropropane-1-sulfinate
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Used as a key reagent in organic synthesis, particularly in 3,3,3-trifluoropropylation reactions. It serves as a source of the 3,3,3-trifluoropropyl (CF3CH2CH2-) group, enabling the introduction of fluorinated alkyl moieties into pharmaceuticals, agrochemicals, and functional materials. Its stability and reactivity under mild conditions make it suitable for late-stage functionalization in drug development. Commonly applied in transition-metal-catalyzed reactions, such as

Used as a key reagent in organic synthesis, particularly in 3,3,3-trifluoropropylation reactions. It serves as a source of the 3,3,3-trifluoropropyl (CF3CH2CH2-) group, enabling the introduction of fluorinated alkyl moieties into pharmaceuticals, agrochemicals, and functional materials. Its stability and reactivity under mild conditions make it suitable for late-stage functionalization in drug development. Commonly applied in transition-metal-catalyzed reactions, such as copper-catalyzed couplings with aryl halides, and radical processes to enhance metabolic stability, lipophilicity, and other physicochemical properties of target molecules.

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