Methyl 4-amino-5-chloro-2-methoxybenzoate

96%

Reagent Code: #87482
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CAS Number 20896-27-9

science Other reagents with same CAS 20896-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.63 g/mol
Formula C₉H₁₀ClNO₃
badge Registry Numbers
MDL Number MFCD01034555
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry, sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a significant role in the production of gastrointestinal drugs, particularly those targeting motility disorders. Its structural properties make it a valuable building block for developing compounds that interact with specific receptors in the digestive system, aiding in the regulation of gastrointestinal functions. Additionally, it is employed in research and development for creating novel therapeutic agents due to its versatile chemical reactivity and ability to form stable derivatives.

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Test Parameter Specification
APPEARANCE White to Off-white to Yellow-green to Gray Solid
Purity (%) 95.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,881.00
inventory 1g
10-20 days ฿4,671.00
inventory 5g
10-20 days ฿18,639.00

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Methyl 4-amino-5-chloro-2-methoxybenzoate
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a significant role in the production of gastrointestinal drugs, particularly those targeting motility disorders. Its structural properties make it a valuable building block for developing compounds that interact with specific receptors in the digestive system, aiding in the regulation of gastrointestinal functions. Additionally, it is employed in research and development for creating novel therapeutic agents due to its versatile chemical reactivity and ability to form stable derivatives.
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