5-Fluoro-2-methoxy-3-nitropyridine

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Reagent Code: #62822
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CAS Number 1211534-27-8

science Other reagents with same CAS 1211534-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.11 g/mol
Formula C₆H₅FN₂O₃
badge Registry Numbers
MDL Number MFCD18260977
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in creating compounds with potential therapeutic effects, such as antiviral or anticancer agents. Additionally, it is utilized in organic chemistry for constructing complex heterocyclic frameworks, which are essential in drug discovery and material science. Its nitro and methoxy 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 ฿4,788.00
inventory 1g
10-20 days ฿23,283.00
inventory 250mg
10-20 days ฿9,324.00
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5-Fluoro-2-methoxy-3-nitropyridine
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in creating compounds with potential therapeutic effects, such as antiviral or anticancer agents. Additionally, it is utilized in organic chemistry for constructing complex heterocyclic frameworks, which are essential in drug discovery and material science. Its nitro and methoxy groups make it a versatile building blo

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in creating compounds with potential therapeutic effects, such as antiviral or anticancer agents. Additionally, it is utilized in organic chemistry for constructing complex heterocyclic frameworks, which are essential in drug discovery and material science. Its nitro and methoxy groups make it a versatile building block for further chemical modifications.

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