5-Bromo-1-butyl-1H-indazole

98%

Reagent Code: #154450
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CAS Number 1280786-85-7

science Other reagents with same CAS 1280786-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.13832 g/mol
Formula C₁₁H₁₃BrN₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of bioactive compounds targeting the central nervous system. It serves as a core structure in the synthesis of cannabinoid receptor modulators, which are investigated for their potential in pain management, anti-inflammatory effects, and neurological disorders. Its alkyl and halogen substitutions make it suitable for further functionalization in medicinal chemistry workflows, especially in structure-activity relationship (SAR) studies. Also utilized in forensic research and reference standards due to its structural similarity to certain psychoactive substances.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,050.00
inventory 5g
10-20 days ฿15,260.00
inventory 25g
10-20 days ฿40,700.00

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5-Bromo-1-butyl-1H-indazole
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Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of bioactive compounds targeting the central nervous system. It serves as a core structure in the synthesis of cannabinoid receptor modulators, which are investigated for their potential in pain management, anti-inflammatory effects, and neurological disorders. Its alkyl and halogen substitutions make it suitable for further functionalization in medicinal chemistry workflows, especially in structure-act

Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of bioactive compounds targeting the central nervous system. It serves as a core structure in the synthesis of cannabinoid receptor modulators, which are investigated for their potential in pain management, anti-inflammatory effects, and neurological disorders. Its alkyl and halogen substitutions make it suitable for further functionalization in medicinal chemistry workflows, especially in structure-activity relationship (SAR) studies. Also utilized in forensic research and reference standards due to its structural similarity to certain psychoactive substances.

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