2509201-09-4 Usage
Uses
Used in Pharmaceutical Industry:
C38H52NOPS is used as a potential pharmaceutical candidate for various applications due to its complex structure and the presence of multiple heteroatoms. C38H52NOPS's ability to interact with biological systems may make it a valuable component in the development of new drugs or therapeutic agents.
Used in Environmental Science:
C38H52NOPS may be used as an environmental marker or tracer in studies related to pollution, ecosystem health, or the behavior of organic compounds in the environment. Its unique chemical signature could help researchers track and understand the movement and impact of pollutants or other substances in natural systems.
Used in Biochemical Research:
C38H52NOPS is used as a research tool in biochemical studies to investigate its interactions with biomolecules and its potential role in cellular processes. Understanding the compound's properties and reactivity could provide insights into fundamental biological mechanisms or lead to the discovery of new biochemical pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 2509201-09-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,5,0,9,2,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2509201-09:
(9*2)+(8*5)+(7*0)+(6*9)+(5*2)+(4*0)+(3*1)+(2*0)+(1*9)=134
134 % 10 = 4
So 2509201-09-4 is a valid CAS Registry Number.
2509201-09-4Relevant articles and documents
Enantioselective Synthesis of Isoxazolines Enabled by Palladium-Catalyzed Carboetherification of Alkenyl Oximes
Chen, Mingjie,Li, Wenbo,Wang, Lei,Wang, Yuzhuo,Zhang, Junliang,Zhang, Kenan
, p. 4421 - 4427 (2020)
Reported here is a highly efficient Pd/Xiang-Phos catalyzed enantioselective carboetherification of alkenyl oximes with either aryl or alkenyl halides, delivering various chiral 3,5-disubstituted and 3,5,5-trisubstituted isoxazolines in good yields with u