7-Bromo-1H-indazole

97%

Reagent Code: #120866
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CAS Number 53857-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.03 g/mol
Formula C₇H₅BrN₂
badge Registry Numbers
MDL Number MFCD07371564
thermostat Physical Properties
Melting Point 123-125°
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its indazole core structure is particularly valuable in the design of drugs targeting enzymes and receptors, making it a crucial component in the creation of potential therapeutic agents. Additionally, it is employed in the development of inhibitors for specific proteins, contributing to advancements in treatments for diseases such as cancer and inflammatory disorders. Its bromine substituent also allows for further functionalization, enabling the creation of diverse derivatives for medicinal chemistry applications.

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Test Parameter Specification
Purity (GC) 97-100
Purity (Titration By AgNO3 After O2 Combustion) 96.5-103.5
Purity (Titration By AgNO3 After O2 Combustion) 96.5-103.5
Appearance White To Tan To Orange Powder
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿300.00
inventory 25g
10-20 days ฿12,460.00
inventory 5g
10-20 days ฿2,980.00
inventory 1g
10-20 days ฿780.00
7-Bromo-1H-indazole
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its indazole core structure is particularly valuable in the design of drugs targeting enzymes and receptors, making it a crucial component in the creation of potential therapeutic agents. Additionally, it is employed in the development of inhibitors for specific proteins, contributing to advancements in treatments for diseases such as cancer and inflammatory disorders. Its bromine substituent also allows for further functionalization, enabling the creation of diverse derivatives for medicinal chemistry applications.
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