Methyl3-amino-5-iodo-2-methylbenzoate

98%

Reagent Code: #213512
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CAS Number 2090331-93-2

science Other reagents with same CAS 2090331-93-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 2919 g/mol
Formula C₉H₁₀INO₂
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 development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building complex aromatic compounds. The presence of both amino and iodo groups enables selective reactions, such as coupling reactions in heterocycle formation or in radiolabeled compound preparation for imaging studies. Also employed in research settings for designing enzyme inhibitors and studying reaction mechanisms in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,930.00
inventory 250mg
10-20 days ฿21,550.00
inventory 1g
10-20 days ฿43,160.00
Methyl3-amino-5-iodo-2-methylbenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building complex aromatic compounds. The presence of both amino and iodo groups enables selective reactions, such as coupling reactions in heterocycle formation or in radiolabeled compound preparation for imaging studies. Also employed i

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building complex aromatic compounds. The presence of both amino and iodo groups enables selective reactions, such as coupling reactions in heterocycle formation or in radiolabeled compound preparation for imaging studies. Also employed in research settings for designing enzyme inhibitors and studying reaction mechanisms in organic synthesis.

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