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1,8(2H,5H)-Acridinedione, 3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-9-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1,8(2H,5H)-Acridinedione, 3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-9-phenyl-

    Cas No: 2769-21-3

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  • 2769-21-3 Structure
  • Basic information

    1. Product Name: 1,8(2H,5H)-Acridinedione, 3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-9-phenyl-
    2. Synonyms:
    3. CAS NO:2769-21-3
    4. Molecular Formula: C23H27NO2
    5. Molecular Weight: 349.473
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2769-21-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. 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)
    10. 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)
    11. 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

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2769-21-3(Hazardous Substances Data)

2769-21-3 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.

Check Digit Verification of cas no

The CAS Registry Mumber 2769-21-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2769-21:
(6*2)+(5*7)+(4*6)+(3*9)+(2*2)+(1*1)=103
103 % 10 = 3
So 2769-21-3 is a valid CAS Registry Number.

2769-21-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,6,6-tetramethyl-9-phenyl-3,4,6,7,9,10-hexahydro-2H,5H-acridine-1,8-dione

1.2 Other means of identification

Product number -
Other names 3,4,6,7-tetrahydro-3,3,6,6-tetramethyl-9-phenylacridine-1,8(2H,5H,9H,10H)-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2769-21-3 SDS

2769-21-3Downstream Products

2769-21-3Relevant articles and documents

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

Muscia, Gisela C.,Buldain, Graciela Y.,Asis, Silvia E.

, p. 1529 - 1532 (2009)

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

Acridine-based thiosemicarbazones as novel inhibitors of mild steel corrosion in 1 M HCl: Synthesis, electrochemical, DFT and Monte Carlo simulation studies

Akpan, Ekemini D.,Isaac, Ibanga O.,Olasunkanmi, Lukman O.,Ebenso, Eno E.,Sherif, El-Sayed M.

, p. 29590 - 29599 (2019)

Electrochemical, surface morphology, density functional theory and Monte Carlo simulation methods were employed in investigating the effects of (2E,2′E)-2,2′-(3,3,6,6-tetramethyl-9-phenyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-diylidene)bis(N-phenylhydrazinecarbothioamide) (IAB-NP), (2E,2′E)-2,2′-(3,3,6,6-tetramethyl-9-phenyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-diylidene)bis(N-(2,4-difluorophenyl)hydrazinecarbothioamide)IAB-ND) and (2E,2′E)-2,2′-(3,3,6,6-tetramethyl-9-phenyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-diylidene)bis(N-(2-fluorophenyl) hydrazinecarbothioamide) (IAB-NF) on mild steel corrosion in 1 M HCl solution. From the studies, compounds IAB-NP, IAB-ND and IAB-NF inhibit mild steel corrosion in the acid and the protection efficiencies were found to increase with the increase in concentration of each compound. At the optimum inhibitor concentration of 1.5 × 10-4 M, the inhibition efficiencies (%) of the compounds are in the order IAB-NF (90.48) > IAB-ND (87.48) > IAB-NP (85.28). Potentiodynamic polarization measurements revealed that all the compounds acted as mixed-type corrosion inhibitors. Experimental data for the adsorption of the studied molecules on a mild steel surface in 1 M HCl fitted into the Langmuir adsorption isotherm and the standard free energies of adsorption (ΔGoads) suggested both physisorption and chemisorption mechanisms. Scanning electron microscopy analyses confirmed the formation of a protective film on the mild steel surface by the inhibitor molecules, resulting in protection of the metal from corrosive electrolyte ions. The experimental findings were corroborated by both theoretical density functional theory and Monte Carlo simulation studies.

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

Pyrko

, p. 1029 - 1031 (2003)

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

Stereodirected catalytic synthesis of perhydroacridines and their isologs from decahydroacridine-1,8-diones

Nikolaeva,Shchekotikhin

, p. 582 - 593 (2004)

The catalytic reduction of decahydroacridine-1,8-diones has been studied under hydrogen pressure in the presence of Raney nickel and with nascent hydrogen from alkaline treatment of nickel-aluminum alloy. Conditions have been developed for the stereodirec

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

Hosseininasab, Fatemeh Sadat,Memarian, Hamid Reza

, (2022/01/11)

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

Alponti, Leonardo H.R.,Picinini, Monize,Urquieta-Gonzalez, Ernesto A.,Corrêa, Arlene G.

, (2020/10/20)

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

Incorporation of Keggin-based H3PW7Mo5O40into bentonite: synthesis, characterization and catalytic applications

Aher, Dipak S.,Khillare, Kiran R.,Shankarwar, Sunil G.

, p. 11244 - 11254 (2021/03/31)

The Keggin-based molybdo-substituted tungstophosphoric acid, H3[PW7Mo5O40]·12H2O, were synthesized and incorporated with a bentonite clay by using a wetness impregnation method. The catalysts were cha

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

Amirnejat, Sara,Javanshir, Shahrzad,Nosrati, Aliakbar

, p. 1186 - 1196 (2021/12/31)

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

Ag/CuO/MCM-48 As a potential catalyst for the synthesis of symmetrical and unsymmetrical polyhydroquinolines

Bazdid-Vahdaty, Narges,Khalili, Behzad,Mamaghani, Manouchehr,Tavakoli, Fateme

, p. 5136 - 5141 (2021/07/13)

Ag/CuO/MCM-48 as a heterogeneous catalyst was efficiently employed in the synthesis of diversely substituted symmetrical and unsymmetrical polyhydroquinoline by a multi-component reaction of arylaldehyde, dimedone, ethyl cyanoacetate and ammonium acetate. This novel method is simple, environmentally friendly, rapid, uses a recyclable catalyst and produces the products in high to excellent yields (83-97%) and lower reaction times (17-35 min). The catalyst can be reused at least 10 times without any appreciable decrease in its catalytic activities.

Synthesis of 1,8-Dioxo-decahydroacridine Derivatives via Ru-Catalyzed Acceptorless Dehydrogenative Multicomponent Reaction

Biswas, Nandita,Srimani, Dipankar

, p. 9733 - 9743 (2021/07/20)

A Ru-catalyzed acceptorless dehydrogenative multicomponent reaction has been developed. This reaction offers a cost-effective and simple operational strategy to synthesize biologically active 1,8-dioxodecahydroacridine derivatives. The protocol provides a wide range of substrate scope and various functional groups are also well tolerated under the reaction condition. To shed light on the mechanistic and kinetic study, some controlled experiments and deuterium labeling experiments were executed. A time-dependent product distribution experiment is also presented and the reaction scale-up is performed to highlight the practical utility of this strategy.

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