873056-60-1 Usage
General Description
2-(3,5-Difluorophenyl)aniline is a chemical compound with the molecular formula C12H9F2N. It is an aromatic amine with a molecular weight of 211.2 g/mol. 2-(3,5-Difluorophenyl)aniline is a derivative of aniline, in which two of the hydrogen atoms on the phenyl ring are replaced by fluorine atoms. It is commonly used in the synthesis of pharmaceuticals, agrochemicals, and dyes. 2-(3,5-Difluorophenyl)aniline is also known for its use as an intermediate in organic synthesis and as a building block in the production of various fine chemicals. It is important for the development of new materials and has potential applications in the fields of medicine and industry. 2-(3,5-Difluorophenyl)aniline should be handled with care, as it may pose hazards if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 873056-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,0,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 873056-60:
(8*8)+(7*7)+(6*3)+(5*0)+(4*5)+(3*6)+(2*6)+(1*0)=181
181 % 10 = 1
So 873056-60-1 is a valid CAS Registry Number.
873056-60-1Relevant articles and documents
Transition-metal-free synthesis of phenanthridinones from biaryl-2-oxamic acid under radical conditions
Yuan, Ming,Chen, Li,Wang, Junwei,Chen, Shenjie,Wang, Kongchao,Xue, Yongbo,Yao, Guangmin,Luo, Zengwei,Zhang, Yonghui
, p. 346 - 349 (2015)
Na2S2O8-promoted decarboxylative cyclization of biaryl-2-oxamic acid for phenanthridinones has been developed. This work illustrates the first example of intramolecular decarboxylative amidation of unactivated arene under transition-metal-free conditions. Additionally, this approach provides an efficient and economical method to access biologically interesting phenanthridinones, an important structure motif in many natural products. (Chemical Equation Presented).
