64026-45-5 Usage
Uses
Used in Flavor and Fragrance Industry:
Dihydro-2,5-dimethylfuran-3(2H)-one is used as a flavoring agent for its pleasant aroma and taste, enhancing the sensory experience of food and beverage products.
Used in Perfumery:
DMF is utilized as a component in the production of fragrances and perfumes, contributing to the creation of complex and appealing scents.
Used in Pharmaceutical Industry:
dihydro-2,5-dimethylfuran-3(2H)-one finds applications in the pharmaceutical sector, potentially serving as a building block or intermediate in the synthesis of various medicinal agents.
Used in Biofuel Research:
Dihydro-2,5-dimethylfuran-3(2H)-one is studied for its potential as a biofuel due to its high energy density and low water solubility, offering an alternative to traditional fossil fuels.
Check Digit Verification of cas no
The CAS Registry Mumber 64026-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,2 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64026-45:
(7*6)+(6*4)+(5*0)+(4*2)+(3*6)+(2*4)+(1*5)=105
105 % 10 = 5
So 64026-45-5 is a valid CAS Registry Number.
64026-45-5Relevant academic research and scientific papers
SPIN DELOCALISATION IN HETEROCYCLIC CAPTODATIVE RADICALS
Nootens, C.,Merenyi, R.,Janousek, Z.,Viehe, H. G.
, p. 1045 - 1054 (2007/10/02)
The open chain and heterocyclic precursors of 12 captodative radicals 1-4 were prepared in order to perform their ESR spectroscopic evaluation.Each of them contains a ketone as a captor substituent and an amino, a thioether or an ether substituent as a dative group.Spectral comparison shows the influence of geometry since 5-membered cd-radicals with thio-groups are more delocalised than their 6-membered or open chain analogues.Interestingly, when cyclic conjugation becomes possible because of an additional double bond such as in 4b, no marked difference of spin delocalisation is observed in comparison with dihydroanalogue 2b.As the dative changes from CH3N- to S- and to O- (in 2b-2d) the delocalisation decreases and the participation of the corresponding carbonyl group increases.
