Methyl 4-amino-3-iodo-5-methylbenzoate

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Reagent Code: #203024
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CAS Number 180624-11-7

science Other reagents with same CAS 180624-11-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.08 g/mol
Formula C₉H₁₀NO₂I
badge Registry Numbers
MDL Number MFCD10703532
thermostat Physical Properties
Boiling Point 383.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.733±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing iodinated aromatic frameworks. The compound is also employed in research settings for radiolabeling studies due to the presence of iodine, enabling imaging and tracer applications. Additionally, it serves as a building block in the preparation of more complex ester and amide derivatives for drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,710.00
inventory 5g
10-20 days ฿42,860.00
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Methyl 4-amino-3-iodo-5-methylbenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing iodinated aromatic frameworks. The compound is also employed in research settings for radiolabeling studies due to the presence of iodine, enabling imaging and tracer applications. Additionally, it serves as a building blo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing iodinated aromatic frameworks. The compound is also employed in research settings for radiolabeling studies due to the presence of iodine, enabling imaging and tracer applications. Additionally, it serves as a building block in the preparation of more complex ester and amide derivatives for drug discovery.

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