852-37-9 Usage
General Description
2-(4-Biphenyl)-5-Phenyloxazole 98% is a specialized chemical compound often used in research and industrial settings. It is characterized by a high purity level of 98% and falls under the category of oxazole, a class of organic compounds that contain a five-membered aromatic ring of three carbon atoms, one oxygen atom, and one nitrogen atom. Its chemical structure consists of a biphenyl group and a phenyl group which are known to influence its chemical properties. The specific applications of 2-(4-Biphenyl)-5-Phenyloxazole can vary widely, but are generally related to its reactivity and the behaviors it displays under certain conditions, which may include emitting fluorescence. Please handle it carefully, as its safety and hazard effects have not been fully investigated.
Check Digit Verification of cas no
The CAS Registry Mumber 852-37-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 852-37:
(5*8)+(4*5)+(3*2)+(2*3)+(1*7)=79
79 % 10 = 9
So 852-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H15NO/c1-3-7-16(8-4-1)17-11-13-19(14-12-17)21-22-15-20(23-21)18-9-5-2-6-10-18/h1-15H
852-37-9Relevant articles and documents
Divergent Conversion of N-Acyl-isoxazol-5(2 H)-ones to Oxazoles and 1,3-Oxazin-6-ones Using Photoredox Catalysis
Mei, Mingjing,Anand, Devireddy,Zhou, Lei
supporting information, p. 3548 - 3553 (2019/05/24)
The fragmentation of N-acyl-isoxazol-5-ones using visible light photoredox catalysis has been disclosed. The catalyst-controlled divergent mechanisms, namely the oxidative and reductive quenching catalytic cycle, are utilized. Various oxazoles and 1,3-oxazin-6-ones are selectively obtained from the same isoxazol-5-one skeleton under mild conditions.
