36516-81-1 Usage
Molecular structure
The compound has a central thiophene ring fused with two benzene rings on either side, forming a heterocyclic structure.
Optoelectronic properties
It exhibits favorable optoelectronic properties, making it suitable for use in organic electronic devices.
Application in devices
It is commonly utilized in organic field-effect transistors and organic solar cells due to its efficient charge transport and high thermal and chemical stability.
Charge transport
The tetraphenylthienothiophene structure allows for efficient charge transport, which is crucial for the performance of electronic devices.
Thermal and chemical stability
The compound demonstrates high thermal and chemical stability, making it a promising material for various technological applications.
Research value
Its unique structure and properties make it a valuable tool for researchers studying organic semiconductors and materials for advanced electronic devices.
Heterocyclic compound
It is classified as a heterocyclic compound, which is a type of organic compound containing a ring structure with at least one heteroatom (an atom other than carbon).
Check Digit Verification of cas no
The CAS Registry Mumber 36516-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,1 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36516-81:
(7*3)+(6*6)+(5*5)+(4*1)+(3*6)+(2*8)+(1*1)=121
121 % 10 = 1
So 36516-81-1 is a valid CAS Registry Number.
36516-81-1Relevant articles and documents
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.
