2854-59-3 Usage
Uses
Used in Pharmaceutical Synthesis:
4-HYDROXY-5-NITROPYRIDAZIN-3(2H)-ONE is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique functional groups allow for versatile chemical reactions, facilitating the creation of new medicinal compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-HYDROXY-5-NITROPYRIDAZIN-3(2H)-ONE serves as a crucial building block for the development of new pesticides and other agricultural chemicals. Its reactivity and structural features contribute to the design of effective and targeted agrochemicals.
Used as a Precursor for Biologically Active Molecules:
4-HYDROXY-5-NITROPYRIDAZIN-3(2H)-ONE is utilized as a precursor in the preparation of biologically active molecules. Its presence in the molecular structure can influence the biological activity, making it an essential component in the development of new pharmaceuticals and other bioactive compounds.
Used in the Synthesis of Heterocyclic Compounds:
As a building block, 4-HYDROXY-5-NITROPYRIDAZIN-3(2H)-ONE is employed in the synthesis of various heterocyclic compounds. Its structural attributes and reactivity make it suitable for the formation of complex heterocyclic systems, which are prevalent in many organic and medicinal chemistry applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2854-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2854-59:
(6*2)+(5*8)+(4*5)+(3*4)+(2*5)+(1*9)=103
103 % 10 = 3
So 2854-59-3 is a valid CAS Registry Number.
2854-59-3Relevant academic research and scientific papers
An efficient synthesis of novel 1,3-oxazolo[4,5-d]pyridazinones
Frolov, Eugene B.,Lakner, Frederick J.,Khvat, Alexandre V.,Ivachtchenko, Alexandre V.
, p. 4693 - 4696 (2007/10/03)
A convenient and versatile synthetic approach to substituted 1,3-oxazolo[4,5-d]pyridazinones is developed. The oxazole ring was formed upon reaction of 5-amino-4-hydroxy-3(2H)-pyridazinone with various carboxylic acid derivatives using a microwave-assisted procedure, which favors the reaction time and purity of the resulting products. The developed methodology is suitable for rapid, parallel, automated synthesis of oxazolopyridazinone libraries.
