5426-04-0 Usage
Uses
Used in Veterinary Medicine:
N'-Hydroxyethanimidamide hydrochloride is used as an antiparasitic agent for the treatment of Babesia and other tick-borne infections in animals. It functions by inhibiting the replication of Babesia parasites, thereby mitigating the impact of these infections on the health of animals.
Used in Parasitic Infection Treatment:
N'-Hydroxyethanimidamide hydrochloride is used as a therapeutic intervention for animals suffering from parasitic infections, specifically those caused by tick-borne pathogens. Its administration via injection ensures targeted delivery to combat the parasites effectively.
Used in Cancer Research:
N'-Hydroxyethanimidamide hydrochloride is used as a subject of investigation in cancer research for its potential antitumor activity. Studies are exploring its ability to inhibit the growth of cancer cells, which could pave the way for new therapeutic approaches in oncology.
Used in Pharmaceutical Development:
In the pharmaceutical industry, N'-Hydroxyethanimidamide hydrochloride is used as a compound of interest in the development of new drugs. Its potential applications in treating parasitic infections and possibly cancer make it a valuable candidate for further research and formulation into medicinal products.
Check Digit Verification of cas no
The CAS Registry Mumber 5426-04-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5426-04:
(6*5)+(5*4)+(4*2)+(3*6)+(2*0)+(1*4)=80
80 % 10 = 0
So 5426-04-0 is a valid CAS Registry Number.
5426-04-0Relevant articles and documents
FORMATION OF 4,5-DIHYDRO-1,2,4-OXADIAZOLES FROM 2-ACYLOXYAMINO OXIMES
Tikhonov, A. Ya.,Belova, N. V.,Volodarskii, L. B.,Gatilov, Yu. V.
, p. 177 - 183 (2007/10/02)
2-Acetoxyamino oximes were obtained by the acylation of 2-hydroxyamino oximes with acetic anhydride.Treatment of 2-acetoxyamino oximes and 2-chloroacetoxyamino oximes with alkali led to rearrangement with the formation of 4,5-dihydro-1,2,4-oxadiazoles.