5-Chloro-4-iodo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine

98%

Reagent Code: #124379
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CAS Number 1040682-76-5

science Other reagents with same CAS 1040682-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 434.82 g/mol
Formula C₁₆H₂₄ClIN₂Si
badge Registry Numbers
MDL Number MFCD09965903
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and iodo substituents, allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. The triisopropylsilyl (TIPS) group serves as a protective moiety for the pyrrolopyridine nitrogen, enhancing stability and directing reactivity during synthetic transformations. Its applications are particularly relevant in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,281.00
inventory 250mg
10-20 days ฿2,700.00
inventory 100mg
10-20 days ฿1,593.00
5-Chloro-4-iodo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and iodo substituents, allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. The triisopropylsilyl (TIPS) group serves as a protective moiety for the pyrrolopyr

This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and iodo substituents, allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. The triisopropylsilyl (TIPS) group serves as a protective moiety for the pyrrolopyridine nitrogen, enhancing stability and directing reactivity during synthetic transformations. Its applications are particularly relevant in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases.

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