3-Bromo-5-nitro-1-trityl-1H-indazole

≥95%

Reagent Code: #118038
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CAS Number 942189-39-1

science Other reagents with same CAS 942189-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 484.34 g/mol
Formula C₂₆H₁₈BrN₃O₂
badge Registry Numbers
MDL Number MFCD17169854
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its unique structure makes it valuable in the creation of pharmaceuticals, particularly in the research and development of new drugs targeting specific biological pathways. The nitro and bromo groups present in the molecule allow for further functionalization, enabling chemists to modify its properties for specific applications. Additionally, it plays a role in the synthesis of indazole derivatives, which are known for their potential biological activities, including anti-inflammatory, anticancer, and antimicrobial effects. Its trityl group provides stability during synthetic processes, making it a useful building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿945.00
inventory 250mg
10-20 days ฿1,602.00
inventory 1g
10-20 days ฿4,302.00

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3-Bromo-5-nitro-1-trityl-1H-indazole
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Used primarily in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its unique structure makes it valuable in the creation of pharmaceuticals, particularly in the research and development of new drugs targeting specific biological pathways. The nitro and bromo groups present in the molecule allow for further functionalization, enabling chemists to modify its properties for specific applications. Additionally, it plays a role in the synthesis of indazole

Used primarily in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its unique structure makes it valuable in the creation of pharmaceuticals, particularly in the research and development of new drugs targeting specific biological pathways. The nitro and bromo groups present in the molecule allow for further functionalization, enabling chemists to modify its properties for specific applications. Additionally, it plays a role in the synthesis of indazole derivatives, which are known for their potential biological activities, including anti-inflammatory, anticancer, and antimicrobial effects. Its trityl group provides stability during synthetic processes, making it a useful building block in medicinal chemistry.

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