4-Iodo-1-(4-methoxybenzyl)-1H-pyrazole

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Reagent Code: #200585
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CAS Number 905751-58-8

science Other reagents with same CAS 905751-58-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.12 g/mol
Formula C₁₁H₁₁IN₂O
badge Registry Numbers
MDL Number MFCD20568993
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating analogs for structure-activity relationship (SAR) studies. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules in medicinal chemistry research. Also utilized in the preparation of radiolabeled derivatives for use in positron emission tomography (PET) imaging due to the presence of iodine, which can be substituted with radioactive isotopes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,160.00
inventory 5g
10-20 days ฿5,710.00

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4-Iodo-1-(4-methoxybenzyl)-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating analogs for structure-activity relationship (SAR) studies. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules in medicinal chemistry research. Also utilized in the pr

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating analogs for structure-activity relationship (SAR) studies. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules in medicinal chemistry research. Also utilized in the preparation of radiolabeled derivatives for use in positron emission tomography (PET) imaging due to the presence of iodine, which can be substituted with radioactive isotopes.

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