Methyl 4-amino-5-iodo-2-methylbenzoate

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Reagent Code: #209222
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CAS Number 672293-33-3

science Other reagents with same CAS 672293-33-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.09 g/mol
Formula C₉H₁₀INO₂
badge Registry Numbers
MDL Number MFCD11112906
inventory_2 Storage & Handling
Density 1.733g/cm3
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of mefenamic acid and related fenamate derivatives. Its structure allows for sequential functionalization, making it valuable in pharmaceutical research for developing analgesic and antipyretic agents. The iodine substituent enables further coupling reactions, such as in palladium-catalyzed cross-couplings, useful in medicinal chemistry for building complex drug molecules. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿840.00
inventory 250mg
10-20 days ฿1,730.00
inventory 1g
10-20 days ฿6,190.00
inventory 5g
10-20 days ฿30,920.00

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Methyl 4-amino-5-iodo-2-methylbenzoate
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Used as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of mefenamic acid and related fenamate derivatives. Its structure allows for sequential functionalization, making it valuable in pharmaceutical research for developing analgesic and antipyretic agents. The iodine substituent enables further coupling reactions, such as in palladium-catalyzed cross-couplings, useful in medicinal chemistry for building complex drug molecules. Also emp

Used as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of mefenamic acid and related fenamate derivatives. Its structure allows for sequential functionalization, making it valuable in pharmaceutical research for developing analgesic and antipyretic agents. The iodine substituent enables further coupling reactions, such as in palladium-catalyzed cross-couplings, useful in medicinal chemistry for building complex drug molecules. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine.

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