tert-Butyl 4-iodo-1H-pyrazole-1-carboxylate

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Reagent Code: #145358
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CAS Number 121669-70-3

science Other reagents with same CAS 121669-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.09 g/mol
Formula C₈H₁₁IN₂O₂
thermostat Physical Properties
Melting Point 67-70°C
Boiling Point 312°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active pyrazole derivatives. Its iodine functionality allows for further transformations via cross-coupling reactions such as Suzuki or Heck couplings, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for the preparation of kinase inhibitors and other targeted therapies. Also utilized in research settings to introduce the pyrazole moiety into larger molecular frameworks, benefiting from the stability provided by the tert-butyl carbamate protecting group.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿410.00
inventory 25g
10-20 days ฿5,990.00
inventory 5g
10-20 days ฿1,670.00

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tert-Butyl 4-iodo-1H-pyrazole-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active pyrazole derivatives. Its iodine functionality allows for further transformations via cross-coupling reactions such as Suzuki or Heck couplings, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for the preparation of kinase inhibitors and other targeted therapies. Also utilized in research settings to introduce the pyrazole moiety

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active pyrazole derivatives. Its iodine functionality allows for further transformations via cross-coupling reactions such as Suzuki or Heck couplings, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for the preparation of kinase inhibitors and other targeted therapies. Also utilized in research settings to introduce the pyrazole moiety into larger molecular frameworks, benefiting from the stability provided by the tert-butyl carbamate protecting group.

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