2-iodo-1-(4-methoxyphenyl)ethanone

≥95%

Reagent Code: #201274
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CAS Number 80336-72-7

science Other reagents with same CAS 80336-72-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.07 g/mol
Formula C₉H₉IO₂
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MDL Number MFCD09032413
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block in the preparation of bioactive molecules due to the presence of both iodo and carbonyl functional groups, which allow for further chemical transformations such as cross-coupling reactions. Commonly employed in the synthesis of analgesics and anti-inflammatory agents. Also utilized in research settings for the development of new synthetic routes and heterocyclic compounds. Its reactivity makes it valuable in forming carbon-carbon bonds under palladium-catalyzed conditions. Handle with care due to potential lachrymatory and irritant properties.

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inventory 1g
10-20 days ฿16,960.00

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2-iodo-1-(4-methoxyphenyl)ethanone
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block in the preparation of bioactive molecules due to the presence of both iodo and carbonyl functional groups, which allow for further chemical transformations such as cross-coupling reactions. Commonly employed in the synthesis of analgesics and anti-inflammatory agents. Also utilized in research settings for the development of new synthetic routes and het

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block in the preparation of bioactive molecules due to the presence of both iodo and carbonyl functional groups, which allow for further chemical transformations such as cross-coupling reactions. Commonly employed in the synthesis of analgesics and anti-inflammatory agents. Also utilized in research settings for the development of new synthetic routes and heterocyclic compounds. Its reactivity makes it valuable in forming carbon-carbon bonds under palladium-catalyzed conditions. Handle with care due to potential lachrymatory and irritant properties.

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