3-(tert-Butyl)-5-iodo-1H-pyrazole

97%

Reagent Code: #44764
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CAS Number 1218791-05-9

science Other reagents with same CAS 1218791-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.08011 g/mol
Formula C₇H₁₁IN₂
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MDL Number MFCD13195724
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of various pharmaceuticals and agrochemicals. Its structure allows for selective modifications, making it valuable in the creation of complex molecules. It is also employed in research for designing inhibitors targeting specific enzymes or receptors, particularly in medicinal chemistry. Additionally, its iodine moiety facilitates further functionalization through cross-coupling reactions, enhancing its utility in constructing diverse chemical architectures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿11,952.00
1g
10-20 days ฿3,681.00
25g
10-20 days ฿51,471.00
3-(tert-Butyl)-5-iodo-1H-pyrazole
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Used primarily in organic synthesis, this compound serves as a key intermediate in the development of various pharmaceuticals and agrochemicals. Its structure allows for selective modifications, making it valuable in the creation of complex molecules. It is also employed in research for designing inhibitors targeting specific enzymes or receptors, particularly in medicinal chemistry. Additionally, its iodine moiety facilitates further functionalization through cross-coupling reactions, enhancing its utility
Used primarily in organic synthesis, this compound serves as a key intermediate in the development of various pharmaceuticals and agrochemicals. Its structure allows for selective modifications, making it valuable in the creation of complex molecules. It is also employed in research for designing inhibitors targeting specific enzymes or receptors, particularly in medicinal chemistry. Additionally, its iodine moiety facilitates further functionalization through cross-coupling reactions, enhancing its utility in constructing diverse chemical architectures.
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