4,4’-Sulfinylbis(iodobenzene)

≥95%

Reagent Code: #237614
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CAS Number 647829-43-4

science Other reagents with same CAS 647829-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.07 g/mol
Formula C₁₂H₈I₂OS
badge Registry Numbers
MDL Number MFCD32876788
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a reagent in organic synthesis, particularly in the formation of hypervalent iodine compounds. It serves as a precursor for generating iodonium salts, which are valuable in electrophilic aromatic substitution and C–H functionalization reactions. Its structure allows for the controlled release of iodo groups, making it useful in pharmaceutical and agrochemical synthesis where selective transformations are required. Also employed in the development of radiolabeled compounds due to the presence of iodine, aiding in imaging and tracer studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,100.00
inventory 5g
10-20 days ฿7,320.00
4,4’-Sulfinylbis(iodobenzene)
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Used as a reagent in organic synthesis, particularly in the formation of hypervalent iodine compounds. It serves as a precursor for generating iodonium salts, which are valuable in electrophilic aromatic substitution and C–H functionalization reactions. Its structure allows for the controlled release of iodo groups, making it useful in pharmaceutical and agrochemical synthesis where selective transformations are required. Also employed in the development of radiolabeled compounds due to the presence of i

Used as a reagent in organic synthesis, particularly in the formation of hypervalent iodine compounds. It serves as a precursor for generating iodonium salts, which are valuable in electrophilic aromatic substitution and C–H functionalization reactions. Its structure allows for the controlled release of iodo groups, making it useful in pharmaceutical and agrochemical synthesis where selective transformations are required. Also employed in the development of radiolabeled compounds due to the presence of iodine, aiding in imaging and tracer studies.

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