80351-05-9 Usage
Chemical class
3-membered heterocyclic compounds
Potential applications
a. Pharmaceutical research and development
b. Synthesis of novel heterocyclic compounds with potential biological activity
Unique structure
1,2-Diazetidin-3-one, 1-(1-methylcyclohexyl)has a 3-membered ring with one nitrogen atom and one carbonyl group
Properties
a. Interesting molecule for further study in various fields of chemistry and medicine
b. Potential for use in the development of new drugs and therapeutic agents
c. May exhibit specific reactivity due to its 3-membered ring and functional groups
Biological activity
The compound may have potential biological activity, warranting further investigation into its effects on biological systems
Synthesis
The compound can be synthesized through various chemical reactions, potentially leading to novel heterocyclic compounds with unique properties and applications
Research focus
Further study of 1,2-Diazetidin-3-one, 1-(1-methylcyclohexyl)may focus on its chemical properties, reactivity, and potential applications in the pharmaceutical and medical fields
Safety considerations
As with any chemical compound, proper handling, storage, and disposal procedures should be followed to ensure the safety of researchers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 80351-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80351-05:
(7*8)+(6*0)+(5*3)+(4*5)+(3*1)+(2*0)+(1*5)=99
99 % 10 = 9
So 80351-05-9 is a valid CAS Registry Number.
80351-05-9Relevant academic research and scientific papers
Synthesis and Reactions of Some 1-Substituted 1,2-Diazetidinones
Taylor, Edward C.,Davies, Huw M. L.
, p. 4415 - 4419 (2007/10/02)
A number of 1,2-diazetidin-3-ones variously substituted at N-1 have been prepared by sodium borohydride reduction of, or addition of methylmagnesium bromide to, 3-oxo-1,2-diazetidinium inner salts (formed by condensation of 3-oxo-1,2-diazetidinium tosylate with carbonyl compounds). 1-Cinnamyl-1,2-diazetidin-3-ones, silylated at N-2, underwent base-promoted alkylation and aldol reactions at C-4.Some unusual dimerization and fragmentation reactions of these aza-β-lactam derivatives have been observed.
