1,4-Diiodo-2,3,5,6-tetramethylbenzene

95%

Reagent Code: #174464
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CAS Number 3268-21-1

science Other reagents with same CAS 3268-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.01 g/mol
Formula C₁₀H₁₂I₂
badge Registry Numbers
MDL Number MFCD00142554
thermostat Physical Properties
Melting Point 137.0-141.0°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a precursor in organic synthesis, particularly in the preparation of functionalized aromatic compounds through cross-coupling reactions. It serves as a building block in the development of advanced materials, including organic semiconductors and liquid crystals, due to its rigid aromatic core and reactive iodine sites. The compound is also employed in the synthesis of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs), where its tetrasubstituted structure helps create well-defined porous networks. Additionally, it finds use in photochemical studies and as a reagent in halogen exchange reactions for generating novel derivatives with tailored electronic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿181.50
inventory 5g
10-20 days ฿759.00

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1,4-Diiodo-2,3,5,6-tetramethylbenzene
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Used as a precursor in organic synthesis, particularly in the preparation of functionalized aromatic compounds through cross-coupling reactions. It serves as a building block in the development of advanced materials, including organic semiconductors and liquid crystals, due to its rigid aromatic core and reactive iodine sites. The compound is also employed in the synthesis of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs), where its tetrasubstituted structure helps create well-def

Used as a precursor in organic synthesis, particularly in the preparation of functionalized aromatic compounds through cross-coupling reactions. It serves as a building block in the development of advanced materials, including organic semiconductors and liquid crystals, due to its rigid aromatic core and reactive iodine sites. The compound is also employed in the synthesis of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs), where its tetrasubstituted structure helps create well-defined porous networks. Additionally, it finds use in photochemical studies and as a reagent in halogen exchange reactions for generating novel derivatives with tailored electronic properties.

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