1-iodo-4-vinyloxybenzene

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Reagent Code: #198804
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CAS Number 1074-57-3

science Other reagents with same CAS 1074-57-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.05 g/mol
Formula C₈H₇IO
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used as a monomer in polymer chemistry, particularly in the synthesis of functional polymers with aromatic and halogenated structures. Its vinyl ether group enables cationic polymerization, allowing the formation of linear or cross-linked materials with unique thermal and optical properties. The presence of iodine facilitates post-polymerization modifications through coupling reactions, such as Heck or Suzuki reactions, enabling the introduction of conjugated systems for applications in organic electronics, sensors, and advanced coatings. Also employed as a building block in the preparation of liquid crystals and photoresponsive materials due to its ability to undergo controlled photochemical transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,970.00
inventory 1g
10-20 days ฿8,730.00
inventory 5g
10-20 days ฿30,600.00

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1-iodo-4-vinyloxybenzene
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Used as a monomer in polymer chemistry, particularly in the synthesis of functional polymers with aromatic and halogenated structures. Its vinyl ether group enables cationic polymerization, allowing the formation of linear or cross-linked materials with unique thermal and optical properties. The presence of iodine facilitates post-polymerization modifications through coupling reactions, such as Heck or Suzuki reactions, enabling the introduction of conjugated systems for applications in organic electroni

Used as a monomer in polymer chemistry, particularly in the synthesis of functional polymers with aromatic and halogenated structures. Its vinyl ether group enables cationic polymerization, allowing the formation of linear or cross-linked materials with unique thermal and optical properties. The presence of iodine facilitates post-polymerization modifications through coupling reactions, such as Heck or Suzuki reactions, enabling the introduction of conjugated systems for applications in organic electronics, sensors, and advanced coatings. Also employed as a building block in the preparation of liquid crystals and photoresponsive materials due to its ability to undergo controlled photochemical transformations.

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