124443-50-1 Usage
General Description
2,4-Imidazolidinedione, 1-acetyl-5-hydroxy- (9CI), also known as Acetohydroxamic acid (AHA), is a chemical compound with the molecular formula C4H7NO3. It is a white, crystalline solid that is soluble in water and has a faint odor. AHA is primarily used as a chelating agent, meaning it can bind and remove metal ions from a solution. It has various industrial applications, including in the production of uranium, as a food preservative, and as a pharmaceutical ingredient. AHA also has medical uses, particularly in the treatment of urinary tract infections by preventing the conversion of urea to ammonia, which inhibits the growth of certain bacteria. However, AHA can be toxic if ingested or inhaled, so careful handling and proper safety precautions are necessary when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 124443-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,4 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 124443-50:
(8*1)+(7*2)+(6*4)+(5*4)+(4*4)+(3*3)+(2*5)+(1*0)=101
101 % 10 = 1
So 124443-50-1 is a valid CAS Registry Number.
124443-50-1Relevant articles and documents
Oxidation of substituted 2-thiouracils and pyrimidine-2-thione with ozone and 3,3-dimethyl-1,2-dioxirane
Claudia, Crestini,Mincione, Enrico,Saladino, Raffaele,Nicoletti, Rosario
, p. 3259 - 3272 (2007/10/02)
Ozone and 3,3-dimethyl-1,2-dioxirane react with substituted 2-thiouracils and pyrimidine-2-thione to afford several interesting desulfurized products. The effect of the solvent, protic as opposed to nonprotic, on the course of oxidation was striking.
Ozonolysis of Uracils in Water
Matsui, Masaki,Nakazumi, Hiroyuki,Kamiya, Kazusaki,Yatome, Chizuko,Shibata, Katsuyoshi,Muramatsu, Hiroshige
, p. 723 - 724 (2007/10/02)
The ozonolysis of uracils unsubstituted at the 1-position gave new 1-acyl-5-hydroxyhydantoins and 5-hydroxyhydantoins in water, while that of 1-substituted uracils gave the corresponding 5-hydroxyhydantoins in low yields.The structure of 1-acetyl-5-hydroxy-5-methylhydantoin was determined by X-ray crystallography.
