Methyl4-amino-5-chloro-2-ethoxybenzoate

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Reagent Code: #213438
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CAS Number 112914-03-1

science Other reagents with same CAS 112914-03-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.66 g/mol
Formula C₁₀H₁₂ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antidepressants such as Vilazodone. It plays a key role in constructing active compounds due to the presence of functional groups like the ester and amino moiety, which allow further chemical modifications. Its chloro and ethoxy substituents influence the electronic and steric properties of the aromatic ring, enhancing selectivity and yield in coupling reactions. Commonly employed in research and development for designing new drug candidates with improved bioavailability and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,560.00
inventory 250mg
10-20 days ฿7,590.00
inventory 1g
10-20 days ฿15,170.00
inventory 5g
10-20 days ฿45,490.00
inventory 10g
10-20 days ฿62,800.00

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Methyl4-amino-5-chloro-2-ethoxybenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antidepressants such as Vilazodone. It plays a key role in constructing active compounds due to the presence of functional groups like the ester and amino moiety, which allow further chemical modifications. Its chloro and ethoxy substituents influence the electronic and steric properties of the aromatic ring, enhancing selectivity and yield in coupling reactions. Commonly employed in research and development fo

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antidepressants such as Vilazodone. It plays a key role in constructing active compounds due to the presence of functional groups like the ester and amino moiety, which allow further chemical modifications. Its chloro and ethoxy substituents influence the electronic and steric properties of the aromatic ring, enhancing selectivity and yield in coupling reactions. Commonly employed in research and development for designing new drug candidates with improved bioavailability and metabolic stability.

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