1332458-85-1 Usage
Structure
Contains a 2,1,3-benzothiadiazole core with boronic acid substituents at positions 4 and 7.
Usage
Commonly employed in organic synthesis and materials science.
Applications
Building Block: Used for the preparation of functionalized molecules and materials.
Organic Electronics: Utilized in the development of organic electronic materials, including organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic photovoltaic devices (OPVs).
Medicinal Chemistry: Studied for potential applications in medicinal chemistry.
Agrochemicals: Investigated for potential use in agrochemical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1332458-85-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,4,5 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1332458-85:
(9*1)+(8*3)+(7*3)+(6*2)+(5*4)+(4*5)+(3*8)+(2*8)+(1*5)=151
151 % 10 = 1
So 1332458-85-1 is a valid CAS Registry Number.
1332458-85-1Relevant articles and documents
An n-channel two-dimensional covalent organic framework
Ding, Xuesong,Chen, Long,Honsho, Yoshihito,Feng, Xiao,Saengsawang, Oraphan,Guo, Jingdong,Saeki, Akinori,Seki, Shu,Irle, Stephan,Nagase, Shigeru,Parasuk, Vudhichai,Jiang, Donglin
, p. 14510 - 14513 (2011)
Co-condensation of metallophthalocyanine with an electron-deficient benzothiadiazole (BTDA) block leads to the formation of a two-dimensional covalent organic framework (2D-NiPc-BTDA COF) that assumes a belt shape and consists of AA stacking of 2D polymer sheets. Integration of BTDA blocks at the edges of a tetragonal metallophthalocyanine COF causes drastic changes in the carrier-transport mode and a switch from a hole-transporting skeleton to an electron-transporting framework. 2D-NiPc-BTDA COF exhibits broad and enhanced absorbance up to 1000 nm, shows panchromatic photoconductivity, is highly sensitive to near-infrared photons, and has excellent electron mobility as high as 0.6 cm2 V-1 s-1.
