Methyl 4-iodo-3-methoxybenzoate

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Reagent Code: #86046
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CAS Number 35387-92-9

science Other reagents with same CAS 35387-92-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.07 g/mol
Formula C₉H₉IO₃
badge Registry Numbers
MDL Number MFCD07367493
thermostat Physical Properties
Boiling Point 324.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed away from light

description Product Description

This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is often employed in the preparation of pharmaceutical intermediates due to its reactive iodine and ester functional groups, which allow for further modifications. Additionally, it serves as a useful reagent in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl or alkyne derivatives. Its methoxy group also makes it a candidate for studies in medicinal chemistry, particularly in the development of compounds targeting specific biological pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿612.00
inventory 250mg
10-20 days ฿1,053.00
inventory 1g
10-20 days ฿2,106.00
inventory 5g
10-20 days ฿8,055.00

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Methyl 4-iodo-3-methoxybenzoate
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This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is often employed in the preparation of pharmaceutical intermediates due to its reactive iodine and ester functional groups, which allow for further modifications. Additionally, it serves as a useful reagent in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl or alkyne derivatives. Its methoxy group also makes it a candidate for studies in medicinal chemistry, particu

This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is often employed in the preparation of pharmaceutical intermediates due to its reactive iodine and ester functional groups, which allow for further modifications. Additionally, it serves as a useful reagent in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl or alkyne derivatives. Its methoxy group also makes it a candidate for studies in medicinal chemistry, particularly in the development of compounds targeting specific biological pathways.

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