132853-90-8 Usage
Molecular structure
The compound has a complex molecular structure consisting of a triazolo cinnoline ring fused with a dione ring, with a benzoyl group and a methoxy-phenyl group attached at specific positions.
Potential biological activities
Due to its unique structure, the compound may have potential biological activities and could be used in various research and pharmaceutical applications.
Benzoyl group
The presence of a benzoyl group suggests that the compound could have a range of potential interactions with biological systems.
Methoxy-phenyl group
The presence of a methoxy-phenyl group also suggests that the compound could have a range of potential interactions with biological systems.
Research and pharmaceutical applications
The compound may be of interest for further study due to its potential interactions with biological systems and its unique structure.
Molecular weight
The molecular weight of the compound is approximately 396.4 g/mol.
Appearance
The compound is likely to be a solid at room temperature, although the exact physical properties are not provided in the material.
Solubility
The solubility of the compound is not provided in the material, but it may be soluble in organic solvents such as dimethyl sulfoxide (DMSO) or methanol.
Stability
The stability of the compound is not provided in the material, but it may be sensitive to light, heat, and moisture, and should be stored under appropriate conditions to maintain its integrity.
Check Digit Verification of cas no
The CAS Registry Mumber 132853-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,5 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132853-90:
(8*1)+(7*3)+(6*2)+(5*8)+(4*5)+(3*3)+(2*9)+(1*0)=128
128 % 10 = 8
So 132853-90-8 is a valid CAS Registry Number.
132853-90-8Relevant academic research and scientific papers
Formation of TetracyclicOxazolidinones from Cycloadducts of Benzylidene Ketones with 4-Phenyl-4,5-dihydro-3H-1,2,4-triazole-3,5-dione (PTAD) by Base-promoted Backbone Participation and Rearrangement
Tanaka, Satoko,Seguchi, Kazuyoshi,Itoh, Kuniaki,Sera, Akira
, p. 2335 - 2340 (2007/10/02)
Alcoholysis and ammonolysis of urazoles 4a-j prepared by a reactions of benzylidene ketones with 4-phenyl-4,5-dihydro-3H-1,2,4-triazole-3,5-dione (PTAD) afforded tricyclic oxazolidinone derivatives 5a-o to moderate yields (16-77percent).The structure of compound 5b was confirmed by a single-crystal X-ray analysis.The reaction proceeded via opening of the urazole ring by initial Michael addition of nucleophiles (solvents) to the enone substructure, followed by participation of the carbonyl group and final skeletal rearrangements.
Novel Base-promoted Addition-Elimination Reaction of Electron-deficient Benzylidene Derivatives with N-Phenyl-1,2,4-triazole-3,5-dione (PTAD)
Seguchi, Kazuyoshi,Tanaka, Satoko
, p. 89 - 90 (2007/10/02)
The reaction of electron-deficient benzylidene derivatives with PTAD afforded the double Diels-Alder product and the Diels-Alder ene product; the latter underwent novel base-induced elimination of phenyl urazole via a stable carbanion.
Base-Induced Addition-Elimination Reactions of Electron-Deficient Vinylarenes Containing a Carbonyl or Ester Group Utilizing 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione (PTAD)
Seguchi, Kazuyoshi,Tanaka, Satoko
, p. 3188 - 3190 (2007/10/02)
The reaction of electron-deficient vinylarenes such as styrylketones and cinnamate with PTAD afforded double Diels-Alder products and Diels-Alder ene products; the latter underwent novel base-induced elimination of 4-phenyl-1,2,4-triazoline-3,5-dione via a stable carbanion.
