27894-44-6 Usage
Uses
Used in Organic Synthesis:
2,5-Bis(hydroxyimino)cyclopentan-1-one is used as a key intermediate in organic synthesis for the production of a variety of chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-Bis(hydroxyimino)cyclopentan-1-one is used as a building block for the development of new drugs, leveraging its chemical properties to create novel medicinal agents.
Used in Agrochemical Industry:
2,5-Bis(hydroxyimino)cyclopentan-1-one is also utilized in the agrochemical sector, where it serves as a precursor for the synthesis of agrochemicals, potentially enhancing crop protection and yield.
Used in Antimicrobial Applications:
2,5-Bis(hydroxyimino)cyclopentan-1-one has been studied for its potential antimicrobial properties, making it a promising candidate for the development of new antimicrobial drugs and treatments.
Used in Antifungal Applications:
Similarly, its antifungal properties are being explored for the creation of new antifungal agents, which could be applied in both medical and agricultural contexts to combat fungal infections and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 27894-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,9 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27894-44:
(7*2)+(6*7)+(5*8)+(4*9)+(3*4)+(2*4)+(1*4)=156
156 % 10 = 6
So 27894-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O3/c8-5-3(6-9)1-2-4(5)7-10/h9-10H,1-2H2/b6-3+,7-4+
27894-44-6Relevant academic research and scientific papers
Metal nitrite: A powerful oxidizing reagent
Baidya, Mahiuddin,Yamamoto, Hisashi
, p. 13880 - 13882 (2011/10/09)
An efficient and simple source of nitroso reagents and their oxidation reactions are described. The combination of a Lewis acid and a metal nitrite was applied to the oxidation of silyl enol ethers. Amino acid and peptide derivatives were easily accessed through in situ C-C bond cleavage of fully substituted silyl enol ethers upon oxidation.
