23386-93-8 Usage
Chemical class
Thieno[3,4-c]thiophene derivatives
Explanation
The compound belongs to a class of heterocyclic compounds containing a thieno[3,4-c]thiophene core structure.
Explanation
It contains two sulfur atoms and a benzene ring, making it a heterocyclic compound.
Explanation
The compound has a benzene ring as part of its core structure.
Explanation
The thieno[3,4-c]thiophene core structure contains two sulfur atoms.
Explanation
The compound is a conjugated molecule due to the alternating single and double bonds in its structure.
Explanation
The compound has unique electronic properties, which make it suitable for applications in organic electronics and optoelectronic devices.
Explanation
Due to its unique electronic properties, the compound has potential applications in these fields.
Explanation
The compound has shown potential in organic semiconductors, which are materials that can conduct electricity and have properties intermediate between those of a conductor and an insulator.
Explanation
The compound can serve as a building block for creating new materials in the field of organic chemistry.
Explanation
The compound is of interest to researchers in these fields due to its unique properties and potential applications.
Heterocyclic compound
Yes
Benzene ring
Present
Sulfur atoms
Two
Phenyl groups
Four
Conjugated molecule
Yes
Electronic properties
Unique
Potential applications
Organic electronics and optoelectronic devices
Organic semiconductors
Potential use
Building block
New materials in organic chemistry
Research interest
Organic chemistry and material science
Check Digit Verification of cas no
The CAS Registry Mumber 23386-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23386-93:
(7*2)+(6*3)+(5*3)+(4*8)+(3*6)+(2*9)+(1*3)=118
118 % 10 = 8
So 23386-93-8 is a valid CAS Registry Number.
23386-93-8Relevant academic research and scientific papers
Synthesis and study of the anodic behavior of 1,3,4,6-tetraaryl-2λ4δ2-thieno[3,4-c] thiophenes
Douadi, Tahar,Cariou, Michel
, p. 509 - 520 (2007/10/03)
Two heterocyclic compounds based on the thieno[3,4-c]thiophene structure with four aryl substituents were prepared and their behavior in electrooxidation studied. These tetraarylthieno[3,4-c]thiophenes were synthesized in three steps starting from 1,3-dibenzoylmethane in the case of 1,3,4,6-tetraphenyl-2λ4δ2-thieno[3,4-c] thiophene 1a and from 1,3-bis(4′-methoxyphenyl)propane-1,3-dione in the case of 1,3,4,6-tetrakis(4′-methoxyphenyl)-2λ4δ 2-thieno[3,4-c]thiophene 1b, a new compound. Both cyclic and hydrodynamic voltamperometric analyses indicate two reversible one-electron oxidation stages for compound 1b, while for compound 1a only the first stage is reversible. The preparative electrooxidation of the two compounds results in the opening of one thiophene ring giving rise to γ-keto-thioketones.
Pyrrolo-1,3,4-thiadiazole Derivatives from Mesomeric Heteropentalenes and Azodicarboxylic Esters
Gotthardt, Hans,Boehm, Frank-Rainer,Brauer, David J.,Weisshuhn, C. Michael,Wilke, C. Jochen
, p. 95 - 104 (2007/10/02)
The mesomeric heteropentalene betaines of type 4,7, and 18 display an unusual reaction behavior against the azodicarboxylic esters 8a-c.Surprisingly, 4 reacts with 8a,b to produce 17a,b, whereas the reaction of 4 with 8c leads to 11 and the novel azomethine imine 15.Also the reaction of 18 with 8a-c gives in two cases 20 or 25 beside the azomethine imine 19.Furthermore, 7 reacts with 8a to form 26, whereas the reaction of 7 with 8c surprisingly yields 29.Spectroscopic data as well as the results of the X-ray analyses of 17a and 19 are consistent with the structures.
