(2-Iodo-4-nitrophenyl)methanol

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Reagent Code: #200584
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CAS Number 500563-90-6

science Other reagents with same CAS 500563-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.03 g/mol
Formula C₇H₆INO₃
badge Registry Numbers
MDL Number MFCD18397985
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and agrochemicals. Its nitro and iodo functional groups allow for selective transformations, such as nitro reduction to amine or potential halogen displacement under appropriate conditions, making it valuable in multi-step synthesis. The compound is also employed in the development of dyes and functionalized aromatic compounds where controlled reactivity is required. Due to the presence of the hydroxyl group, it can undergo esterification or etherification to build more complex molecules. Its structure supports applications in research settings for constructing heterocyclic systems and bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿990.00
inventory 1g
10-20 days ฿3,890.00
inventory 5g
10-20 days ฿18,610.00

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(2-Iodo-4-nitrophenyl)methanol
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Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and agrochemicals. Its nitro and iodo functional groups allow for selective transformations, such as nitro reduction to amine or potential halogen displacement under appropriate conditions, making it valuable in multi-step synthesis. The compound is also employed in the development of dyes and functionalized aromatic compounds where controlled reactivity is required. Due to the presence of the hydroxy

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and agrochemicals. Its nitro and iodo functional groups allow for selective transformations, such as nitro reduction to amine or potential halogen displacement under appropriate conditions, making it valuable in multi-step synthesis. The compound is also employed in the development of dyes and functionalized aromatic compounds where controlled reactivity is required. Due to the presence of the hydroxyl group, it can undergo esterification or etherification to build more complex molecules. Its structure supports applications in research settings for constructing heterocyclic systems and bioactive molecules.

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