Introduction of CAS:3268-21-1 | 1,4-DIIODO-2,3,5,6-TETRAMETHYLBENZENE
4-diiodo-2,3,5, 6-tetramethylbenzene is an organic compound with the formula C10H10I2. It consists of two positions on the benzene ring being replaced by iodine atoms, while methyl groups are present at positions 2, 3, 5, and 6.
Materials science: Due to the special properties of its molecular structure, this compound may be used in the field of materials science, for example as a fluorescent marker, a precursor of organic semiconductor materials, or a synthetic intermediate of functional compounds.
Specification of CAS:3268-21-1 | 1,4-DIIODO-2,3,5,6-TETRAMETHYLBENZENE
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ITEMS |
SPECIFICATION |
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Density |
1.942±0.06 g/cm3(Predicted) |
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Boiling point |
343.2±37.0 °C(Predicted) |
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Color |
White to almost white |
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Form |
powder crystal |
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Storage condition |
Keep in dark place,Sealed in dry,Room Temperature |
Research Application of CAS:3268-21-1 | 1,4-DIIODO-2,3,5,6-TETRAMETHYLBENZENE
Sterically Crowded Tetraarylbenzenes
A series of bulky 1,4-diiodo-2,3,5,6-tetraarylbenzenes has been synthesized, showcasing the utility of 1,4-Diiodo-2,3,5,6-tetramethylbenzene in creating sterically crowded benzenes. These materials demonstrate interesting structural distortions under steric pressures, relevant in the study of molecular structure and interactions (Shah et al., 2003).
Crystallographic Studies
The compound has been studied for its crystallographic properties, such as in the case of Diiododurene, where interesting molecular packing and interactions were observed. This is pivotal for understanding molecular geometries and interactions in solid-state chemistry (Britton & Gleason, 2003).
Reactions with Fuming Nitric Acid
Research has explored the reaction of tetramethylbenzonitriles, including compounds similar to 1,4-Diiodo-2,3,5,6-tetramethylbenzene, with fuming nitric acid. This research contributes to the understanding of chemical reactions and synthesis pathways in organic chemistry (Suzuki et al., 1978).
Suzuki-Miyaura Mono-Arylation
The compound has been used in research involving the Suzuki-Miyaura mono-arylation of symmetrical diiodo(hetero)arenes, demonstrating its utility in organic synthesis and the development of new chemical methodologies (Sapegin & Krasavin, 2018).
Synthesis of Naphthalenes
It has been involved in novel synthetic routes to octasubstituted naphthalenes, showcasing its role in complex organic synthesis and the creation of new organic compounds (Zhou et al., 2004).
Hydrogen Sorption in Metal-Organic Frameworks
The compound has been used in the synthesis of metal-organic frameworks, particularly for studying hydrogen sorption, which is crucial in materials science and energy storage research (Rowsell et al., 2004).
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