86129-90-0 Usage
Molecular structure
1-cyclohexyl-3,3-diphenyl-4-(2-phenylethenyl)azetidin-2-one has a complex molecular structure, which includes a cyclohexyl group, two phenyl groups, and a 2-phenylethenyl group.
Classification
It is a member of the azetidine class of compounds.
Potential applications
The compound has potential applications in pharmacology and medicinal chemistry.
Analgesic properties
May help in relieving pain.
Anti-inflammatory properties
May help in reducing inflammation.
Anticonvulsant properties
May help in preventing or treating convulsions or seizures.
Mechanism of action
The precise mechanism of action for 1-cyclohexyl-3,3-diphenyl-4-(2-phenylethenyl)azetidin-2-one has yet to be fully elucidated.
Therapeutic potential
Its unique structure makes it an intriguing target for further research and potential drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 86129-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,2 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86129-90:
(7*8)+(6*6)+(5*1)+(4*2)+(3*9)+(2*9)+(1*0)=150
150 % 10 = 0
So 86129-90-0 is a valid CAS Registry Number.
86129-90-0Relevant academic research and scientific papers
Halogenated Ketenes. 38. Cycloaddition of α,β-Unsaturated Imines with Ketenes To Yield Both β- and δ-Lactams
Brady, William T.,Shieh, C. H.
, p. 2499 - 2502 (2007/10/02)
The cycloaddition of various types of α,β-unsaturated imines with diphenyl- and dichloroketenes yields both (2 + 2) and (4 + 2) cycloaddition products, i. e., β-lactams and δ-lactams, respectively.The cycloaddition products are dependent upon substitution in the imine and the ketene.The δ-lactams derived from dichloroketene are easily dehydrochlorinated to the corresponding 2-pyridones.All of the results are consistent with a two-step cycloaddition process involving a dipolar intermediate.
