Ethyl-4-methylamino-3-nitrobenzoate

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Reagent Code: #47736
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CAS Number 71254-71-2

science Other reagents with same CAS 71254-71-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.21 g/mol
Formula C₁₀H₁₂N₂O₄
badge Registry Numbers
MDL Number MFCD09746194
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in organic synthesis as an intermediate for the production of pharmaceuticals and agrochemicals. It serves as a key building block in the development of compounds with potential therapeutic properties, particularly in the creation of molecules targeting neurological disorders. Its nitro and ester functional groups make it valuable in reactions like reduction, esterification, and amidation, enabling the formation of more complex structures. Additionally, it is utilized in research settings for studying reaction mechanisms and developing novel chemical entities.

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Test Parameter Specification
Appearance Light yellow to yellow powder or crystals
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,300.00
inventory 1g
10-20 days ฿1,330.00

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Ethyl-4-methylamino-3-nitrobenzoate
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Used primarily in organic synthesis as an intermediate for the production of pharmaceuticals and agrochemicals. It serves as a key building block in the development of compounds with potential therapeutic properties, particularly in the creation of molecules targeting neurological disorders. Its nitro and ester functional groups make it valuable in reactions like reduction, esterification, and amidation, enabling the formation of more complex structures. Additionally, it is utilized in research settings

Used primarily in organic synthesis as an intermediate for the production of pharmaceuticals and agrochemicals. It serves as a key building block in the development of compounds with potential therapeutic properties, particularly in the creation of molecules targeting neurological disorders. Its nitro and ester functional groups make it valuable in reactions like reduction, esterification, and amidation, enabling the formation of more complex structures. Additionally, it is utilized in research settings for studying reaction mechanisms and developing novel chemical entities.

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