Methyl 4-iodo-1-methyl-1H-pyrazole-3-carboxylate

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Reagent Code: #209217
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CAS Number 75092-25-0

science Other reagents with same CAS 75092-25-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.04 g/mol
Formula C₆H₇IN₂O₂
badge Registry Numbers
MDL Number MFCD19703827
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing pyrazole-based drug candidates. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the exploration of structure-activity relationships in drug design. Also utilized in agrochemical research for developing novel pesticides and herbicides due to the pyrazole moiety's inherent biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿780.00
inventory 1g
10-20 days ฿3,060.00
inventory 5g
10-20 days ฿13,160.00

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Methyl 4-iodo-1-methyl-1H-pyrazole-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing pyrazole-based drug candidates. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the exploration of structure-activity relationships in drug design. Also utilized

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing pyrazole-based drug candidates. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the exploration of structure-activity relationships in drug design. Also utilized in agrochemical research for developing novel pesticides and herbicides due to the pyrazole moiety's inherent biological activity.

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