93598-65-3 Usage
Uses
Used in Organic Synthesis:
(2Z)-3-cyclohexyl-2-(cyclohexylimino)-6-methyl-2,3-dihydro-4H-1,3-oxazin-4-one is used as a key intermediate in organic synthesis for the creation of complex organic molecules. Its unique structure and functional groups make it a versatile building block for the development of new compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2Z)-3-cyclohexyl-2-(cyclohexylimino)-6-methyl-2,3-dihydro-4H-1,3-oxazin-4-one is used as a starting material for the design and synthesis of pharmaceutical agents. Its derivatives have been studied for their potential applications in medicine, highlighting its importance in drug discovery and development.
Used in Drug Development:
(2Z)-3-cyclohexyl-2-(cyclohexylimino)-6-methyl-2,3-dihydro-4H-1,3-oxazin-4-one is employed as a component in the development of different types of drugs. Its properties and structure make it suitable for creating molecules with therapeutic potential, contributing to the advancement of novel pharmaceuticals.
Used in Material Science:
Although not explicitly mentioned in the provided materials, given the compound's structural features and potential for molecular interactions, it can also be inferred that (2Z)-3-cyclohexyl-2-(cyclohexylimino)-6-methyl-2,3-dihydro-4H-1,3-oxazin-4-one may find applications in material science, potentially serving as a component in the development of new materials with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 93598-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93598-65:
(7*9)+(6*3)+(5*5)+(4*9)+(3*8)+(2*6)+(1*5)=183
183 % 10 = 3
So 93598-65-3 is a valid CAS Registry Number.
93598-65-3Relevant academic research and scientific papers
Regioselective synthesis of 2-iminooxazinones from dioxinones and carbodiimides
Johnston, Jeffrey R.,West
, p. 5479 - 5482 (2013/01/13)
Iminooxazinones are readily formed via microwave heating of dioxinones in the presence of carbodiimides. Unsymmetrically substituted carbodiimides generally react with high or complete regioselectivity, allowing for assembly of the target ring systems wit
Reaction of 2,2-dimethyl-1,3-dioxin-4-ones with Imines, Carbodiimides, and Isocyanates
Sato, Masayuki,Ogasawara, Hiromichi,Kato, Tetsuzo
, p. 2602 - 2608 (2007/10/02)
The ring transformation of 2,2-dimethyl-1,3-dioxin-4-ones (1) to nitrogen heterocycles was studied.Heating of 1 whith imines such as Schiff bases gave rise to cycloadducts of imines to acylketenes (2), i.e., 3,4-dihydro-1,3-oxazin-4-one derivatives
