105404-91-9

Usage

Uses

Used in Organic Synthesis:
2,8-Diiododibenzothiophene is used as a building block in organic synthesis for the creation of a variety of chemical compounds. Its specific chemical properties and reactivity contribute to the formation of new molecules with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,8-Diiododibenzothiophene is utilized as a key intermediate in the synthesis of drugs. Its unique structure and reactivity allow for the development of new pharmaceutical agents with potential therapeutic benefits.
Used in Agrochemical Industry:
2,8-Diiododibenzothiophene is employed as a starting material in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the creation of effective compounds for agricultural applications.
Used in Materials Science:
In the field of materials science, 2,8-Diiododibenzothiophene is used as a component in the development of advanced materials with specific properties. Its incorporation into these materials can enhance their performance and contribute to the advancement of various technologies.

Upstream product

• 31574-87-5 2,8-dibromodibenzothiophene 
• 132-65-0 dibenzothiophene 

Downstream Products

• 404906-09-8 2,8-bis(phenylethynyl)dibenzothiophene 
• 951791-28-9 2-(4-{4-[2-(2-butoxy-ethoxy)-ethoxy]-phenylethynyl}-phenylethynyl)-8-(4-iodo-phenylethynyl)-dibenzothiophene 5,5-dioxide 
• 951791-24-5 2,8-bis((4-iodophenyl)ethynyl)dibenzothiophene 5,5-dioxide 
• 951791-10-9 2-{4-[2-(2-butoxy-ethoxy)-ethoxy]-phenylethynyl}-8-iodo-dibenzothiophene 5,5-dioxide 

Relevant academic research and scientific papers

Synthesis and characterization of carbazole-based dendrimers as bipolar host materials for green phosphorescent organic light emitting diodes

A group of novel, carbazole-based dendrimers comprised of the electron-accepting dibenzothiophene core and the electron-donating oligo-carbazole dendrons, namely G1SF and G2SF, are synthesized utilizing the Ullmann C-N coupling reaction. The dendrimers ar

Cyanines as new fluorescent probes for DNA detection and two-photon excited bioimaging

A series of cyanine fluorophores based on fused aromatics as an electron donor for DNA sensing and two-photon bioimaging were synthesized, among which the carbazole-based biscyanine exhibits high sensitivity and efficiency as a fluorescent light-up probe for dsDNA, which shows selective binding toward the AT-rich regions. The synergetic effect of the bischromophoric skeleton gives a several-fold enhancement in a two-photon absorption cross-section as well as a 25- to 100-fold enhancement in two-photon excited fluorescence upon dsDNA binding.

IODINATION PROCESS, MONOMER AND POLYMER

The present invention relates to processes for the preparation of iodinated compounds of formula (I): (Formula (I)) wherein R1 is the same or different in each occurrence and is a substituent; m independently in each occurrence is 0, 1, 2 or 3; and X independently in each occurrence is NR2, PR2, -CR22-, -SiR22, O or S wherein R2 is the same or different in each occurrence and is a substituent.

NEW DIBENZOFURANS AND DIBENZOTHIOPHENES

The present invention relates to compounds of formula (I) which are characterized in that they are substituted by at least one nitrile substituted carbazolyl group and their use in electronic devices, especially electroluminescent devices. When used as el

Synthesis and Structure-Linear and Structure-Nonlinear Optical Properties of Multi-Dipolar Zigzag Oligoaryleneethynylenes

A novel series of monodisperse, multi-dipolar zigzag oligoaryleneethynylenes DA(n) and D-Ar-A(n), bearing electron-donating dibenzothiophene and electron-accepting dibenzothiophene dioxide as arenes, with up to six charge-transfer (dipolar) units