225512-46-9 Usage
Uses
Used in Textile Industry:
1,4-Bis-(2-ethylhexyl)-2,5-diiodobenzene is used as a dye for textiles, providing vibrant colors and enhancing the visual appeal of fabrics. Its high solubility in organic solvents allows for easy application and even distribution of color throughout the material.
Used in Plastic and Polymer Production:
In the plastic and polymer industry, 1,4-bis-(2-ethylhexyl)-2,5-diiodobenzene is employed as a stabilizer. Its presence helps to prevent the degradation of plastics, ensuring their durability and longevity.
Used in Organic Compound Synthesis:
This chemical compound is also used as an intermediate in the synthesis of various organic compounds. Its unique structure and properties make it a valuable component in the creation of a range of different chemical products.
Used in Adhesive and Coating Formulation:
1,4-Bis-(2-ethylhexyl)-2,5-diiodobenzene is utilized in the formulation of certain types of adhesives and coatings, where its properties contribute to the overall performance and effectiveness of these products.
Safety Precautions:
It is important to handle 1,4-bis-(2-ethylhexyl)-2,5-diiodobenzene with caution, as it can be harmful if ingested or if it comes into contact with the skin or eyes. Proper safety measures, such as wearing protective gear and following appropriate handling procedures, should be taken to minimize the risk of exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 225512-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,5,1 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 225512-46:
(8*2)+(7*2)+(6*5)+(5*5)+(4*1)+(3*2)+(2*4)+(1*6)=109
109 % 10 = 9
So 225512-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H36I2/c1-5-9-11-17(7-3)13-19-15-22(24)20(16-21(19)23)14-18(8-4)12-10-6-2/h15-18H,5-14H2,1-4H3
225512-46-9Relevant academic research and scientific papers
Linker-Dependent Singlet Fission in Tetracene Dimers
Korovina, Nadezhda V.,Joy, Jimmy,Feng, Xintian,Feltenberger, Cassidy,Krylov, Anna I.,Bradforth, Stephen E.,Thompson, Mark E.
supporting information, p. 10179 - 10190 (2018/07/30)
Separation of triplet excitons produced by singlet fission is crucial for efficient application of singlet fission materials. While earlier works explored the first step of singlet fission, the formation of the correlated triplet pair state, the focus of
Structural study of the thermochromic transition in poly(2,5-dialkyl-/p- phenyleneethynylene)s
Lebouch, Nolwenn,Garreau, Sebastien,Louarn, Guy,Belletete, Michel,Durocher, Gilles,Leclerc, Mario
, p. 9631 - 9637 (2008/02/01)
The solvatochromic and thermochromic properties of poly(2,5-di-2′- ethylhexyl-p-phenyleneethynylene) have been investigated. While some important changes were observed in UV - vis absorption, calorimetric, and X-ray measurements, temperature-dependent FTI
