70524-43-5 Usage
Uses
Used in Pharmaceutical Industry:
[1,1-Biphenyl]-2,5-diol,4-bromo-(9CI) is used as an intermediate compound for the synthesis of various pharmaceutical products due to its unique chemical properties and reactivity.
Used in Agrochemical Industry:
[1,1-Biphenyl]-2,5-diol,4-bromo-(9CI) is used as a building block for the development of new agrochemicals, potentially enhancing the effectiveness of pesticides and other agricultural chemicals.
Used in Material Science:
[1,1-Biphenyl]-2,5-diol,4-bromo-(9CI) is used as a component in the creation of novel materials with specific properties, such as improved stability or reactivity, for various applications in material science.
Further research and testing may be required to fully understand and explore the potential uses and applications of [1,1-Biphenyl]-2,5-diol,4-bromo-(9CI) in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 70524-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,2 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70524-43:
(7*7)+(6*0)+(5*5)+(4*2)+(3*4)+(2*4)+(1*3)=105
105 % 10 = 5
So 70524-43-5 is a valid CAS Registry Number.
70524-43-5Relevant academic research and scientific papers
Visible-Light-Induced, Catalyst-Free Radical Arylations of Arenes and Heteroarenes with Aryldiazonium Salts
Fürst, Michael C. D.,Gans, Eva,B?ck, Michael J.,Heinrich, Markus R.
supporting information, p. 15312 - 15315 (2017/10/20)
In the absence of a photocatalyst and other additives, the radical arylation of diverse arenes and heteroarenes has been achieved with aryldiazonium salts under visible-light irradiation from a blue light-emitting diode (LED). Although the course of some reactions can be rationalized by the formation of strongly light-absorbing charge-transfer (CT) complexes between the diazonium ion and the aromatic substrate, several further examples indicated that the simple presence of an aromatic substrate, showing only weak interactions to the diazonium ion, is fully sufficient to enable product formation.
