4-Iodo-2-((tosyloxy)methyl)phenyl4-methylbenzenesulfonate

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Reagent Code: #201048
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CAS Number 2682115-56-4

science Other reagents with same CAS 2682115-56-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 558.41 g/mol
Formula C₂₁H₁₉IO₆S₂
badge Registry Numbers
MDL Number MFCD32856771
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex aromatic compounds and pharmaceuticals. Its dual sulfonate ester functionality allows for selective substitution reactions, enabling stepwise introduction of different groups onto the aromatic ring. The iodo group serves as a handle for cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in the synthesis of biaryl structures commonly found in bioactive molecules. Commonly employed in research settings for the development of functionalized phenyl derivatives with potential applications in medicinal chemistry and materials science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿860.00
inventory 250mg
10-20 days ฿1,550.00
inventory 1g
10-20 days ฿4,500.00
inventory 10g
10-20 days ฿39,460.00
4-Iodo-2-((tosyloxy)methyl)phenyl4-methylbenzenesulfonate
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Used as a key intermediate in organic synthesis, particularly in the preparation of complex aromatic compounds and pharmaceuticals. Its dual sulfonate ester functionality allows for selective substitution reactions, enabling stepwise introduction of different groups onto the aromatic ring. The iodo group serves as a handle for cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in the synthesis of biaryl structures commonly found in bioactive molecules. Commonly employed in rese

Used as a key intermediate in organic synthesis, particularly in the preparation of complex aromatic compounds and pharmaceuticals. Its dual sulfonate ester functionality allows for selective substitution reactions, enabling stepwise introduction of different groups onto the aromatic ring. The iodo group serves as a handle for cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in the synthesis of biaryl structures commonly found in bioactive molecules. Commonly employed in research settings for the development of functionalized phenyl derivatives with potential applications in medicinal chemistry and materials science.

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