Ethyl 7-bromo-1H-indazole-3-carboxylate

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Reagent Code: #50368
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CAS Number 885279-56-1

science Other reagents with same CAS 885279-56-1

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scatter_plot Molecular Information
Weight 269.0947 g/mol
Formula C₁₀H₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD07371617
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of indazole-based compounds, which are explored for their potential therapeutic applications, including anti-inflammatory, anticancer, and antimicrobial agents. Additionally, it is employed in organic synthesis to construct complex heterocyclic frameworks, aiding in the discovery of new drug candidates. Its bromo and ester functional groups make it a versatile building block for further chemical modifications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,090.00

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Ethyl 7-bromo-1H-indazole-3-carboxylate
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of indazole-based compounds, which are explored for their potential therapeutic applications, including anti-inflammatory, anticancer, and antimicrobial agents. Additionally, it is employed in organic synthesis to construct complex heterocyclic frameworks, aiding in the discovery of new drug

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of indazole-based compounds, which are explored for their potential therapeutic applications, including anti-inflammatory, anticancer, and antimicrobial agents. Additionally, it is employed in organic synthesis to construct complex heterocyclic frameworks, aiding in the discovery of new drug candidates. Its bromo and ester functional groups make it a versatile building block for further chemical modifications.

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