3-(4-Iodo-1H-pyrazol-1-yl)pyridine

95%

Reagent Code: #198585
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CAS Number 1306604-89-6

science Other reagents with same CAS 1306604-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.06 g/mol
Formula C₈H₆IN₃
badge Registry Numbers
MDL Number MFCD19597013
thermostat Physical Properties
Boiling Point 350.7±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.90±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry, light-proof

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of targeted cancer therapies. Its structure supports binding to specific enzyme active sites, making it valuable in creating compounds that modulate protein activity involved in tumor growth. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds. Additionally, it serves as a building block in the preparation of radiolabeled tracers for positron emission tomography (PET) imaging, leveraging the iodine atom for isotope substitution.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,980.00
inventory 1g
10-20 days ฿68,750.00

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3-(4-Iodo-1H-pyrazol-1-yl)pyridine
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of targeted cancer therapies. Its structure supports binding to specific enzyme active sites, making it valuable in creating compounds that modulate protein activity involved in tumor growth. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds. Additionally, it

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of targeted cancer therapies. Its structure supports binding to specific enzyme active sites, making it valuable in creating compounds that modulate protein activity involved in tumor growth. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds. Additionally, it serves as a building block in the preparation of radiolabeled tracers for positron emission tomography (PET) imaging, leveraging the iodine atom for isotope substitution.

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