58556-77-7 Usage
Uses
Used in Organic Synthesis:
2,7-Diiodonaphthalene is used as a building block in organic synthesis for the creation of more complex molecules, leveraging its high reactivity in chemical reactions.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,7-Diiodonaphthalene is used as a key intermediate in the synthesis of various drugs, contributing to the development of new medicinal compounds.
Used in Dye Manufacturing:
2,7-Diiodonaphthalene is utilized in the production of dyes, where its chemical properties are harnessed to create a range of colorants for different applications.
Used in Agrochemicals:
2,7-Diiodonaphthalene serves as a crucial component in the formulation of agrochemicals, aiding in the development of products for agricultural use.
Used in Materials Science:
It is applied in materials science for the research and development of new materials with specific properties, taking advantage of its chemical structure and reactivity.
Used in Organic Electronic Devices:
2,7-Diiodonaphthalene is used in the field of organic electronics, where its properties are explored for potential applications in devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).
Check Digit Verification of cas no
The CAS Registry Mumber 58556-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58556-77:
(7*5)+(6*8)+(5*5)+(4*5)+(3*6)+(2*7)+(1*7)=167
167 % 10 = 7
So 58556-77-7 is a valid CAS Registry Number.
58556-77-7Relevant academic research and scientific papers
FUSED THIOPHENE MOLECULE AND p-TYPE SEMICONDUCTOR FILM AND ELECTRONIC DEVICE
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Paragraph 0099, (2021/12/03)
To provide a fused thiophene molecule having further sufficiently high hole mobility. Disclosed is a fused thiophene molecule that has seven aromatic rings containing three thiophene rings in one molecule and in which the seven aromatic rings have one or two naphthalene structures. And, semiconductor devices including a layer using the fused thiophene molecule are disclosed.
Intramolecular interactions in diiodonaphthalenes
Novak, Igor,Jiang, Huiming,Kovac, Branka
, p. 480 - 484 (2007/10/03)
The synthesis and the electronic structure of isomeric di-iodonaphthalenes is described. The electronic structure has been investigated by HeI/HeII photoelectron spectroscopy and non-Koopmans' quantum chemical calculations. The influence of the topology of iodine substitution on the electronic structure is discussed. Special emphasis is placed on elucidating the role of intramolecular iodine-iodine interactions.
