3-(iodomethyl)oxane

≥95%

Reagent Code: #198718
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CAS Number 32730-60-2

science Other reagents with same CAS 32730-60-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.0554 g/mol
Formula C₆H₁₁IO
badge Registry Numbers
MDL Number MFCD30623825
thermostat Physical Properties
Boiling Point 229.1±13.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.645±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex molecules, particularly in pharmaceutical and agrochemical industries. The iodomethyl group acts as a reactive site for nucleophilic substitution reactions, enabling the formation of carbon-oxygen and carbon-carbon bonds. It is also employed in the development of functionalized heterocyclic compounds, where the oxane ring can act as a protecting group or structural motif. Due to its reactivity, it is valuable in route design for target-oriented synthesis, especially where halogenated ethers are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,000.00
inventory 100mg
10-20 days ฿8,000.00
3-(iodomethyl)oxane
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex molecules, particularly in pharmaceutical and agrochemical industries. The iodomethyl group acts as a reactive site for nucleophilic substitution reactions, enabling the formation of carbon-oxygen and carbon-carbon bonds. It is also employed in the development of functionalized heterocyclic compounds, where the oxane ring can act as a protecting group or structural motif. Due to its reactivity,

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex molecules, particularly in pharmaceutical and agrochemical industries. The iodomethyl group acts as a reactive site for nucleophilic substitution reactions, enabling the formation of carbon-oxygen and carbon-carbon bonds. It is also employed in the development of functionalized heterocyclic compounds, where the oxane ring can act as a protecting group or structural motif. Due to its reactivity, it is valuable in route design for target-oriented synthesis, especially where halogenated ethers are required.

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