761405-37-2 Usage
Uses
Used in Organic Synthesis:
2,8-Diboronodibenzo[b,d]thiophene, 3,6-Diborono-9-thiafluorene is used as a building block for [the synthesis of complex organic molecules] due to [its unique boron and sulfur containing structure that allows for various chemical reactions].
Used in Materials Chemistry:
2,8-Diboronodibenzo[b,d]thiophene, 3,6-Diborono-9-thiafluorene is used as a component in [the development of new materials] for [its potential to enhance material properties such as electrical conductivity or light emission].
Used in Organic Electronics:
2,8-Diboronodibenzo[b,d]thiophene, 3,6-Diborono-9-thiafluorene is used as a semiconductor material for [organic electronic devices] because of [its electronic properties that are suitable for charge transport and semiconducting behavior].
Used in Optoelectronic Devices:
2,8-Diboronodibenzo[b,d]thiophene, 3,6-Diborono-9-thiafluorene is used as an active layer material for [optoelectronic devices such as organic light-emitting diodes (OLEDs) and photovoltaic cells] for [its light-emitting or light-absorbing characteristics].
Used in Research Applications:
2,8-Diboronodibenzo[b,d]thiophene, 3,6-Diborono-9-thiafluorene is used as a subject of study for [exploring new chemical reactions and material properties] in [the advancement of organic chemistry and related fields].
Check Digit Verification of cas no
The CAS Registry Mumber 761405-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,4,0 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 761405-37:
(8*7)+(7*6)+(6*1)+(5*4)+(4*0)+(3*5)+(2*3)+(1*7)=152
152 % 10 = 2
So 761405-37-2 is a valid CAS Registry Number.
761405-37-2Relevant academic research and scientific papers
Jin, Enquan,Du, Chun,Wang, Ming,Li, Weiwei,Li, Cuihong,Wei, Hedi,Bo, Zhishan
, p. 7843 - 7854,12 (2012)
Three D-A alternating copolymers P1-3 with 3,7-linked 2,8-bis(alkoxy) dibenzothiophene as the donor unit and benzothiadiazole (P1 and P2) or 3,4-bis(octyloxy)benzothiadiazole (P3) as the acceptor unit have been designed and synthesized. P1-3 show two broa
