2769-21-3

Basic information

• Product Name: 1,8(2H,5H)-Acridinedione, 3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-9-phenyl-
• CAS NO: 2769-21-3
• Molecular Formula: C23H27NO2
• Molecular Weight: 349.473
• Mol File: 2769-21-3.mol
• Article Data: 95

Chemical Properties

• CAS DataBase Reference: 1,8(2H,5H)-Acridinedione, 3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-9-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,8(2H,5H)-Acridinedione, 3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-9-phenyl-(2769-21-3)
• EPA Substance Registry System: 1,8(2H,5H)-Acridinedione, 3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-9-phenyl-(2769-21-3)

Safety Data

• Hazardous Substances Data: 2769-21-3(Hazardous Substances Data)

Usage

Molecular structure

The compound has a complex molecular structure consisting of an acridinedione moiety and a hexahydro-3,3,6,6-tetramethyl-9-phenyl group.

Acridinedione moiety

This is a fused heterocyclic ring system, which contributes to the compound's unique properties.

Hexahydro-3,3,6,6-tetramethyl-9-phenyl group

This part of the molecule consists of a cyclohexane ring with methyl and phenyl substituents.

Potential applications

Due to its unique structure and properties, the compound may have potential applications in various fields such as organic synthesis, pharmaceuticals, and materials science.

Further research

More research is needed to fully understand the compound's potential uses and effects.

Molecular weight

The molecular weight of the compound is approximately 365.48 g/mol.

Appearance

The compound is likely to be a solid, although its exact appearance (e.g., color, crystal structure) is not specified in the provided material.

Solubility

The solubility of the compound in various solvents is not specified in the provided material, but it may vary depending on the specific solvent and conditions.

Stability

The stability of the compound under different conditions (e.g., temperature, pressure, exposure to light or air) is not specified in the provided material. Further research would be needed to determine its stability profile.

Upstream product

• 100-52-7 benzaldehyde 
• 873-95-0 1-amino-5,5-dimethylcyclohexen-3-one 
• 123-54-6 acetylacetone 
• 126-81-8 dimedone 
• 31771-33-2 2-phenyl-4,4,6-trimethyltetrahydro-(2H)-1,3-oxazine 
• 492-70-6 1,2-diphenyl-1,2-ethanediol 
• 100-51-6 benzyl alcohol 
• 889-31-6 5,5-dimethyl-3-benzylamino-2-cyclohexen-1-one 
• 19419-23-9 2,2'-phenylmethylene-bis(5,5-dimethylcyclohexane-1,3-dione) 
• 631-61-8 ammonium acetate 
• 868992-00-1 10-hydroxy-3,3,6,6-tetramethyl-9-phenyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione 
• 30122-00-0 α-chloro-benzylisocyanate 
• 1001588-86-8 7,7-dimethyl-4-phenyl-4,6,7,8-tetrahydro-2H-1,3-benzoxazine-2,5(3H)-dione 
• 183737-75-9 10-benzyl-3,4,6,7-tetrahydro-3,3,6,6-tetramethyl-9-phenylacridine-1,8(2H,5H,9H,10H)-dione 

Relevant articles and documents

Only acridine derivative from Hantzsch-type one-pot three-component reactions

A three-component Hantzsch-type condensation of different anilines with dimedone and benzaldehyde leads to the formation of a unique acridine derivative with an unusual breaking of a C-N bond. The reaction was also carried out employing rapid microwave or

Reaction of 3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-diones with lithium aluminum hydride

The corresponding 3,3,6,6,-tetramethyl-1,2,3,4,5,6,7,8-octahydroacridines have been obtained by the interaction of 3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione, its 9-Ph- and 9-p-MeOC6H4-substituted derivative

Efficient synthesis of decahydroacridine-1,8-diones and polyhydroquinolines using the step-wise method

Various symmetrical and unsymmetrical decahydroacridine-1,8-dione and polyhydroquinoline derivatives were synthesized via two-step cyclocondensation reactions. The advantages of this step-wise addition of reactants in comparison with other one-pot reactions are avoiding the formation of 2 or 3 undesired by-products, therefore allowing cleaner work up of reaction. The important factor of this effective cyclocondensation method is that the prepared β-enaminone component was added dropwise to the solution, in which the Knoevenagel condensation product is slowly being formed by reaction of aldehyde molecule and 1,3-dicarbonyl compounds. The results of the proposed step-wise method are compared and discussed with those obtained in the one-pot reactions.

USY-zeolite catalyzed synthesis of 1,4-dihydropyridines under microwave irradiation: structure and recycling of the catalyst

The Hantzsch three-component reaction is the best-known multicomponent reaction, affording dihydropyridines which have been employed therapeutically and also as visible‐light photoredox catalysts. In this work we report the application of an ultra-stable

Preparation, Antibacterial Activity, and Catalytic Application of Magnetic Graphene Oxide-Fucoidan in the Synthesis of 1,4-Dihydropyridines and Polyhydroquinolines

Polymer-coated magnetic nanoparticles are emerging as a useful tool for a variety of applications, including catalysis. In the present study, fucoidan-coated magnetic graphene oxide was synthesized using a natural sulfated polysaccharide. The prepared BaF