1-(2-Phenylethynyl)-1,2-benziodoxol-3(1H)-one

95%

Reagent Code: #227535
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CAS Number 181934-31-6

science Other reagents with same CAS 181934-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.14 g/mol
Formula C₁₅H₉IO₂
badge Registry Numbers
MDL Number MFCD31699849
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used primarily as a hypervalent iodine reagent in organic synthesis, this compound enables efficient and selective alkyne transfer reactions. It is especially valuable in the generation of vinyl cations and in metal-free carbon–carbon bond-forming processes. Its stability and reactivity make it suitable for use in the synthesis of conjugated enynes and in cycloaddition reactions. It also serves as a versatile reagent in radical reactions and photoredox catalysis, allowing functionalization under mild conditions. Due to its ability to act as an electrophilic alkyne source, it is widely applied in the construction of complex molecular architectures found in natural products and pharmaceuticals.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,170.00
250mg
10-20 days ฿6,320.00
1g
10-20 days ฿20,290.00
5g
10-20 days ฿87,120.00
1-(2-Phenylethynyl)-1,2-benziodoxol-3(1H)-one
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Used primarily as a hypervalent iodine reagent in organic synthesis, this compound enables efficient and selective alkyne transfer reactions. It is especially valuable in the generation of vinyl cations and in metal-free carbon–carbon bond-forming processes. Its stability and reactivity make it suitable for use in the synthesis of conjugated enynes and in cycloaddition reactions. It also serves as a versatile reagent in radical reactions and photoredox catalysis, allowing functionalization under mild con

Used primarily as a hypervalent iodine reagent in organic synthesis, this compound enables efficient and selective alkyne transfer reactions. It is especially valuable in the generation of vinyl cations and in metal-free carbon–carbon bond-forming processes. Its stability and reactivity make it suitable for use in the synthesis of conjugated enynes and in cycloaddition reactions. It also serves as a versatile reagent in radical reactions and photoredox catalysis, allowing functionalization under mild conditions. Due to its ability to act as an electrophilic alkyne source, it is widely applied in the construction of complex molecular architectures found in natural products and pharmaceuticals.

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