98778-16-6 Usage
Uses
Used in Pharmaceutical Synthesis:
2,3-Piperazinedione,1,4-dimethyl-,dioxime,(E,Z)-(9CI) is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used as a Chelating Agent in Agriculture:
In agriculture, 2,3-Piperazinedione,1,4-dimethyl-,dioxime,(E,Z)-(9CI) can be used as a chelating agent for metal ions. Its ability to form stable complexes with metal ions can help improve the bioavailability and uptake of essential nutrients by plants, leading to enhanced crop growth and yield.
Used in Industrial Chemistry:
2,3-Piperazinedione,1,4-dimethyl-,dioxime,(E,Z)-(9CI) also has potential applications in industrial chemistry. Its chelating properties can be utilized in various chemical processes, such as catalysis, where it can help improve reaction efficiency and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 98778-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,7 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98778-16:
(7*9)+(6*8)+(5*7)+(4*7)+(3*8)+(2*1)+(1*6)=206
206 % 10 = 6
So 98778-16-6 is a valid CAS Registry Number.
98778-16-6Relevant academic research and scientific papers
Synthesis and Chemistry of Some Furazano- and Furoxanopiperazines
Willer, Rodney L.,Moore, Donald W.
, p. 5123 - 5127 (2007/10/02)
A series of N,N'-disubstituted furazano- and furoxanopiperazines 1a-d and 2b-d have been synthesized from N,N'-disubstituted 2,3-piperazinedione dioximes 5a-d by base-promoted dehydration and by basic potassium ferricyanide oxidation, respectively.The N,N'-disubstituted 2,3-piperazinedione dioximes were synthesized by reacting the appropriate N,N'-disubstituted ethylenediamine with dichloroglyoxime.Also studied was the reaction of 3,4-diaminofurazan with glyoxal and formaldehyde.The compounds have been studied by 1H and 13C NMR spectroscopy.
