507484-47-1 Usage
Description
Propanedinitrile, (6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene)is a chemical compound with the molecular formula C11H7BrN2O. It is a nitrile derivative with a 6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene group attached to a propanedinitrile molecule. Propanedinitrile, (6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene)is known for its versatile reactivity and potential for forming new compounds.
Uses
Used in Chemical Synthesis:
Propanedinitrile, (6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene)is used as a key intermediate in chemical synthesis for the production of various organic compounds. Its unique structure and reactivity make it a valuable building block in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
Propanedinitrile, (6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene)is used as a starting material or intermediate in the development of pharmaceuticals. Its potential applications in drug discovery and design are being explored due to its unique chemical properties and reactivity.
Used in Agrochemicals:
Propanedinitrile, (6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene)is used in the development of agrochemicals, such as pesticides and herbicides. Its reactivity and potential for forming new compounds make it a promising candidate for the creation of novel and effective agrochemical products.
Used in Materials Science:
Propanedinitrile, (6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene)is used in materials science for the development of new materials with unique properties. Its potential applications in this field are being investigated, as it may contribute to the creation of advanced materials with improved performance characteristics.
Further research is needed to fully understand the properties and potential uses of Propanedinitrile, (6-bromo-2,3-dihydro-3-oxo-1H-inden-1-ylidene)in various industries. Its versatile reactivity and potential for forming new compounds make it a promising compound for future applications.
Check Digit Verification of cas no
The CAS Registry Mumber 507484-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,4,8 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 507484-47:
(8*5)+(7*0)+(6*7)+(5*4)+(4*8)+(3*4)+(2*4)+(1*7)=161
161 % 10 = 1
So 507484-47-1 is a valid CAS Registry Number.
507484-47-1Relevant articles and documents
Configurational Isomers Induced Significant Difference in All-Polymer Solar Cells
Wang, Hengtao,Chen, Hui,Xie, Weicheng,Lai, Hanjian,Zhao, Tingxing,Zhu, Yulin,Chen, Lin,Ke, Chunxian,Zheng, Nan,He, Feng
, (2021/04/22)
The design of polymer acceptors plays an essential role in the performance of all-polymer solar cells. Recently, the strategy of polymerized small molecules has achieved great success, but most polymers are synthesized from the mixed monomers, which seriously affects batch-to-batch reproducibility. Here, a method to separate γ-Br-IC or δ-Br-IC in gram scale and apply the strategy of monomer configurational control in which two isomeric polymeric acceptors (PBTIC-γ-2F2T and PBTIC-δ-2F2T) are produced is reported. As a comparison, PBTIC-m-2F2T from the mixed monomers is also synthesized. The γ-position based polymer (PBTIC-γ-2F2T) shows good solubility and achieves the best power conversion efficiency of 14.34% with a high open-circuit voltage of 0.95?V when blended with PM6, which is among the highest values recorded to date, while the δ-position based isomer (PBTIC-δ-2F2T) is insoluble and cannot be processed after parallel polymerization. The mixed-isomers based polymer, PBTIC-m-2F2T, shows better processing capability but has a low efficiency of 3.26%. Further investigation shows that precise control of configuration helps to improve the regularity of the polymer chain and reduce the π–π stacking distance. These results demonstrate that the configurational control affords a promising strategy to achieve high-performance polymer acceptors.
