((2-Iodoethoxy)methyl)benzene

98%

Reagent Code: #200456
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CAS Number 54555-84-9

science Other reagents with same CAS 54555-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.09 g/mol
Formula C₉H₁₁IO
badge Registry Numbers
MDL Number MFCD10574996
inventory_2 Storage & Handling
Storage 2-8℃, away from light, dry, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. As a primary alkyl iodide, its iodo group serves as an excellent leaving group for nucleophilic substitution reactions and enables various cross-coupling reactions (e.g., with organometallic reagents) to form carbon-carbon bonds, facilitating the assembly of complex molecular structures, including those incorporating aromatic systems. The ether linkage enhances stability and modulates solubility, aiding in the design of molecules with tailored polarity. Additionally, it is utilized in the synthesis of radiolabeled compounds for medical imaging, where the iodine position allows for isotopic exchange or substitution with radioactive isotopes such as iodine-125.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,620.00
inventory 5g
10-20 days ฿6,480.00
inventory 10g
10-20 days ฿12,690.00
inventory 25g
10-20 days ฿20,390.00
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((2-Iodoethoxy)methyl)benzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. As a primary alkyl iodide, its iodo group serves as an excellent leaving group for nucleophilic substitution reactions and enables various cross-coupling reactions (e.g., with organometallic reagents) to form carbon-carbon bonds, facilitating the assembly of complex molecular structures, including those incorporating aromatic systems. The ether linkage enhances stability and modul

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. As a primary alkyl iodide, its iodo group serves as an excellent leaving group for nucleophilic substitution reactions and enables various cross-coupling reactions (e.g., with organometallic reagents) to form carbon-carbon bonds, facilitating the assembly of complex molecular structures, including those incorporating aromatic systems. The ether linkage enhances stability and modulates solubility, aiding in the design of molecules with tailored polarity. Additionally, it is utilized in the synthesis of radiolabeled compounds for medical imaging, where the iodine position allows for isotopic exchange or substitution with radioactive isotopes such as iodine-125.

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