52386-40-0 Usage
Uses
Used in Veterinary Medicine:
3-METHYL-1,2,4-OXADIAZOL-5-OL is used as an anthelmintic and insecticidal agent for controlling a broad spectrum of internal and external parasites in livestock and companion animals. It is effective against gastrointestinal nematodes, lungworms, mites, and lice, making it an important tool in parasite control and prevention programs in agricultural and veterinary settings.
Used in Parasite Control and Prevention Programs:
3-METHYL-1,2,4-OXADIAZOL-5-OL is used as a long-lasting efficacy agent in parasite control and prevention programs, ensuring the health and well-being of livestock and companion animals by reducing the impact of parasitic infections.
Used in Various Formulations:
3-METHYL-1,2,4-OXADIAZOL-5-OL is used in different formulations such as oral drenches, injectables, and topical products for easy administration in various animal species, providing flexibility and convenience in its application for effective parasite management.
Check Digit Verification of cas no
The CAS Registry Mumber 52386-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,8 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52386-40:
(7*5)+(6*2)+(5*3)+(4*8)+(3*6)+(2*4)+(1*0)=120
120 % 10 = 0
So 52386-40-0 is a valid CAS Registry Number.
52386-40-0Relevant academic research and scientific papers
Kinetics of base-catalysed hydrolysis and cyclisation of substituted acetamide and benzamide O-(phenoxycarbonyl)oximes
Mindl, Jaromir,Kavalek, Jaromir,Strakova, Helena,Sterba, Vojeslav
, p. 1641 - 1653 (2007/10/03)
The reaction kinetics of acetamide O-(4-nitrophenoxycarbonyl)oxime have been studied in aqueous buffers at pH 2-11. At pH > 9, the pH dependence of kobs is linear with slope 1, the cyclisation to 3-methyl-1,2,4-oxadiazol-5(4H)-one and 4-nitrophenol being the only reaction. At pH obs on pH has been used to determine the rate equation and to propose the reaction mechanism. The cyclisation kinetics of substituted benzamide O-(phenoxycarbonyl)oximes have been studied in the pH range from 9.25 to 11. The reaction mechanism has been proposed based on the ρ constants found. In the first reaction step, the proton is split off from the NH2 group; the subsequent, rate-limiting step involves simultaneous N-C bond formation and C-O bond splitting.
