1611002-56-2 Usage
Uses
Used in Materials Science:
5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole is used as a component in the development of new materials due to its unique structure and properties. Its incorporation can potentially enhance the performance of materials in various applications.
Used in Organic Electronics:
In the field of organic electronics, 5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole is used as a key component in the design and synthesis of organic electronic devices. Its properties can contribute to improved device performance and functionality.
Used in Pharmaceutical Research:
5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its unique structure can be leveraged to develop new drugs with potential therapeutic applications.
Used in Chemical Research:
5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole is used as a subject of study in chemical research, where its synthesis and characterization can provide insights into the development of new materials and compounds for various industrial and scientific purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 1611002-56-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,1,0,0 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1611002-56:
(9*1)+(8*6)+(7*1)+(6*1)+(5*0)+(4*0)+(3*2)+(2*5)+(1*6)=92
92 % 10 = 2
So 1611002-56-2 is a valid CAS Registry Number.
1611002-56-2Relevant academic research and scientific papers
Effects of fluorination on the electrochromic performance of benzothiadiazole-based donor - Acceptor copolymers
Neo, Wei Teng,Ong, Kok Haw,Lin, Ting Ting,Chua, Soo-Jin,Xu, Jianwei
, p. 5589 - 5597 (2015/06/08)
A series of thiophene and benzothiadiazole-based copolymers (PDAT-DTBT) is synthesized through Stille coupling polymerization with two mono- and di-fluorinated benzothiadiazole analogues: PDAT-DTBT-F (1F) and PDAT-DTBT-2F (2F). The introduction of fluorine atoms onto the conjugated polymer backbone is found to have a pronounced effect on the optical, electrochemical and morphological properties, which in turn, influences the electrochromic performance of the fabricated absorption/transmission type devices greatly. All the polymers switch reversibly between the colored neutral states (green/blue) to transmissive oxidized states. Systematic enhancement in the reduction process to sub-second speeds (2 C-1) and substantially improved ambient stability are observed upon fluorination of electron acceptors. Long-term stability testing of the PDAT-DTBT-F electrochromic device is carried out for up to 10 000 repeated redox cycles between the applied potentials of +1.6 and -1.6 V, without the observation of significant degradation.
