Ethyl 4-amino-2-methylbenzoate

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Reagent Code: #183690
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CAS Number 74450-59-2

science Other reagents with same CAS 74450-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.22 g/mol
Formula C₁₀H₁₃NO₂
badge Registry Numbers
MDL Number MFCD08458830
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and anti-inflammatory agents. It serves as a building block in organic reactions due to the presence of both amino and ester functional groups, enabling coupling reactions and ring modifications. Commonly employed in the development of dyes and agrochemicals as well, thanks to its aromatic structure and reactivity. Its derivatives are also explored in medicinal chemistry for potential bioactive properties.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿920.00
inventory 25g
10-20 days ฿2,000.00
inventory 100g
10-20 days ฿7,820.00
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Ethyl 4-amino-2-methylbenzoate
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and anti-inflammatory agents. It serves as a building block in organic reactions due to the presence of both amino and ester functional groups, enabling coupling reactions and ring modifications. Commonly employed in the development of dyes and agrochemicals as well, thanks to its aromatic structure and reactivity. Its derivatives are also explored in medicinal chemistry for potentia

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and anti-inflammatory agents. It serves as a building block in organic reactions due to the presence of both amino and ester functional groups, enabling coupling reactions and ring modifications. Commonly employed in the development of dyes and agrochemicals as well, thanks to its aromatic structure and reactivity. Its derivatives are also explored in medicinal chemistry for potential bioactive properties.

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