75397-90-9 Usage
Chemical structure
A heterocyclic compound with a bicyclic structure, containing a diazabicyclohexene ring fused with an enone group.
Substituents
Substituted with a methylphenyl group at the 3-position and two phenyl groups at the 4and 6-positions.
Applications
Used in organic synthesis as a versatile building block for the preparation of various biologically active molecules and pharmaceuticals.
Potential applications
May have potential applications in medicinal chemistry and material science due to its unique structure and reactivity.
Safety precautions
Should be handled and used with proper safety precautions due to its potential hazards.
Reactivity
The unique structure of the compound may contribute to its reactivity in various chemical reactions, making it a valuable building block in organic synthesis.
Biological activity
The compound may be used to create biologically active molecules, which could have potential applications in the development of new drugs and therapies.
Structural complexity
The bicyclic structure and multiple substituents contribute to the structural complexity of the compound, which may influence its properties and reactivity.
Synthesis
The compound can be synthesized through various chemical reactions, making it a useful building block in the preparation of more complex molecules.
Hazards
As with any chemical compound, it is important to be aware of the potential hazards associated with handling and using 1,3-Diazabicyclo[2.2.0]hex-5-en-2-one, 3-(4-methylphenyl)-4,6-diphenyl-, and to follow proper safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 75397-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75397-90:
(7*7)+(6*5)+(5*3)+(4*9)+(3*7)+(2*9)+(1*0)=169
169 % 10 = 9
So 75397-90-9 is a valid CAS Registry Number.
75397-90-9Relevant academic research and scientific papers
Novel Synthesis of 2,4-Diarylquinolines by Photochemical followed by Thermal Transformations of 1,4,6-Triarylpyrimidin-2(1H)-ones
Nishio, Takehiko,Omote, Yoshimori
, p. 1773 - 1775 (2007/10/02)
The 2,4-diarylquinolines (3) were obtained in a one-pot synthesis by photochemical and subsequent thermal reactions of 1,4,6-triarylpyrimidin-2(1H)-ones (1) in fair yield.The quinolines (3) were formed via thermal cycloreversion, followed by electrocyclic ring-closure, of the 1,3-diazabicyclohex-5-en-2-ones (2), which were produced by photochemical electrocyclization of the pyrimidin-2(1H)-ones (1).
NOVEL SYNTHESIS OF 2,4-DIPHENYLQUINOLINES
Nishio, Takehiko,Katahira, Katsuhiro,Omote, Yoshimori
, p. 2825 - 2826 (2007/10/02)
2,4-Diphenylquinolines (3) were quantitatively prepared by heating of 3-aryl-4,6-diphenyl-2-oxo-1,3-diazabicyclohex-5-enes (2), which were obtained by photochemical electrocyclization of 1-aryl-4,6-diphenyl-2(1H)-pyrimidin-2-ones (1), in benzene at reflux temperature.
