5-Chloro-6-methoxy-1H-indazole

≥95%

Reagent Code: #161915
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CAS Number 1082041-58-4

science Other reagents with same CAS 1082041-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.61 g/mol
Formula C₈H₇ClN₂O
badge Registry Numbers
MDL Number MFCD11007885
thermostat Physical Properties
Boiling Point 344.8±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its indazole core, which is known for favorable binding to biological targets. Commonly employed in research settings to design compounds with anti-inflammatory, antiviral, and antiproliferative activities. Its chloro and methoxy substituents allow for further functionalization, enabling structure-activity relationship studies in drug discovery programs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,650.00
inventory 250mg
10-20 days ฿15,470.00
inventory 1g
10-20 days ฿38,760.00

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5-Chloro-6-methoxy-1H-indazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its indazole core, which is known for favorable binding to biological targets. Commonly employed in research settings to design compounds with anti-inflammatory, antiviral, and antiproliferative activities. Its chloro and methoxy substituents allow for further functionalization, enabling structure-activity re

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its indazole core, which is known for favorable binding to biological targets. Commonly employed in research settings to design compounds with anti-inflammatory, antiviral, and antiproliferative activities. Its chloro and methoxy substituents allow for further functionalization, enabling structure-activity relationship studies in drug discovery programs.

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