5-Bromo-2-(4-chlorobenzyl)-2H-indazole

≥95%

Reagent Code: #149895
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CAS Number 1205548-67-9

science Other reagents with same CAS 1205548-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.6 g/mol
Formula C₁₄H₁₀BrClN₂
thermostat Physical Properties
Boiling Point 468.6±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.53±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structural features enable selective binding to enzyme active sites, making it valuable in drug discovery programs focused on targeted therapies. It is also employed in research settings to design and optimize new bioactive molecules with potential anti-inflammatory and antitumor activities. Due to its halogenated aromatic framework, it serves as a building block in cross-coupling reactions for generating diverse compound libraries in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿27,360.00
inventory 5mg
10-20 days ฿87,390.00

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5-Bromo-2-(4-chlorobenzyl)-2H-indazole
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structural features enable selective binding to enzyme active sites, making it valuable in drug discovery programs focused on targeted therapies. It is also employed in research settings to design and optimize new bioactive molecules with potential anti-inflammatory and antitumor activities. Due to its halogenated aromatic framework, it serves a

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structural features enable selective binding to enzyme active sites, making it valuable in drug discovery programs focused on targeted therapies. It is also employed in research settings to design and optimize new bioactive molecules with potential anti-inflammatory and antitumor activities. Due to its halogenated aromatic framework, it serves as a building block in cross-coupling reactions for generating diverse compound libraries in medicinal chemistry.

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