5-Iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole

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Reagent Code: #200477
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CAS Number 1311197-82-6

science Other reagents with same CAS 1311197-82-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.09 g/mol
Formula C₈H₁₁IN₂O
badge Registry Numbers
MDL Number MFCD19237232
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The tetrahydropyranyl (THP) group acts as a protecting group for the pyrazole nitrogen, enabling selective functionalization at the 5-iodo position and facilitating multi-step syntheses. This structure makes it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Additionally, the iodine substituent allows for replacement with radioactive isotopes, making it suitable for labeling and tracer studies in research settings for imaging purposes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿630.00
inventory 1g
10-20 days ฿2,040.00
inventory 5g
10-20 days ฿8,840.00
inventory 10g
10-20 days ฿14,410.00
inventory 25g
10-20 days ฿36,000.00

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5-Iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The tetrahydropyranyl (THP) group acts as a protecting group for the pyrazole nitrogen, enabling selective functionalization at the 5-iodo position and facilitating multi-step syntheses. This structure makes it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The tetrahydropyranyl (THP) group acts as a protecting group for the pyrazole nitrogen, enabling selective functionalization at the 5-iodo position and facilitating multi-step syntheses. This structure makes it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Additionally, the iodine substituent allows for replacement with radioactive isotopes, making it suitable for labeling and tracer studies in research settings for imaging purposes.

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