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719-54-0,MFCD00005024
Catalog No.:AA003DRH

719-54-0 | 10-Methyl-9(10H)-acridone

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Quantity
  
250mg
98%
in stock  
$18.00   $13.00
- +
1g
95%
in stock  
$37.00   $26.00
- +
5g
95%
in stock  
$79.00   $55.00
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25g
95%
in stock  
$278.00   $195.00
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100g
95%
in stock  
$809.00   $567.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003DRH
Chemical Name:
10-Methyl-9(10H)-acridone
CAS Number:
719-54-0
Molecular Formula:
C14H11NO
Molecular Weight:
209.2432
MDL Number:
MFCD00005024
SMILES:
Cn1c2ccccc2c(=O)c2c1cccc2
Properties
Properties
 
BP:
361.3°C at 760 mmHg  
Form:
Solid  
MP:
204-207 °C  
Refractive Index:
1.5780 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
263  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
XLogP3:
3.1  

Downstream Synthesis Route

[1]Zhang,Bo;Cui,Yuxin;Jiao,Ning[ChemicalCommunications,2012,vol.48,#37,p.4498-4500]

[2]Jiang,Hong;Liu,You-Cheng;Li,Jing;Wang,Guan-Wu;Wu,Yun-Dong;Wang,Quan-Ming;Mak,ThomasC.W.[ChemicalCommunications,2002,#8,p.882-883]

[3]Pan,Decheng;Wang,Yiqing;Li,Meichao;Hu,Xinquan;Sun,Nan;Jin,Liqun;Hu,Baoxiang;Shen,Zhenlu[Synlett,2019,vol.30,#2,p.218-224]

[4]CurrentPatentAssignee:ZHEJIANGUNIVERSITYOFTECHNOLOGY-CN109336813,2019,ALocationinpatent:Paragraph0025-0042

[5]Chinchilla,Rafael;Torregrosa-Chinillach,Alejandro[Molecules,2021,vol.26,#4]

[6]Zhou,Jiacheng;Li,Meichao;Li,Tianci;Li,Chunmei;Hu,Xinquan;Jin,Liqun;Sun,Nan;Hu,Baoxiang;Shen,Zhenlu[Tetrahedron,2021,vol.82]

[7]Shukla,Deepak;Rege,Francisde;Wan,Peter;Johnston,LindaJ.[JournalofPhysicalChemistry,1991,vol.95,#25,p.10240-10246]

[8]Pictet;Patry[ChemischeBerichte,1902,vol.35,p.2536]

[9]Fukuzumi,Shunichi;Ishikawa,Masashi;Tanaka,Toshio[JournaloftheChemicalSociety.PerkintransactionsII,1989,p.1037-1046]

[10]Shukla,Deepak;Rege,Francisde;Wan,Peter;Johnston,LindaJ.[JournalofPhysicalChemistry,1991,vol.95,#25,p.10240-10246]

[11]Lee,JungYoon;Lee,Yong-Min;Kotani,Hiroaki;Nam,Wonwoo;Fukuzumi,Shunichi[ChemicalCommunications,2009,#6,p.704-706]

[12]Jung,Jieun;Ohkubo,Kei;Prokop-Prigge,KatharineA.;Neu,HeatherM.;Goldberg,DavidP.;Fukuzumi,Shunichi[InorganicChemistry,2013,vol.52,#23,p.13594-13604]

[13]Jung,Jieun;Ohkubo,Kei;Goldberg,DavidP.;Fukuzumi,Shunichi[JournalofPhysicalChemistryA,2014,vol.118,#32,p.6223-6229]

[14]Devi,Tarali;Lee,Yong-Min;Jung,Jieun;Sankaralingam,Muniyandi;Nam,Wonwoo;Fukuzumi,Shunichi[AngewandteChemie-InternationalEdition,2017,vol.56,#13,p.3510-3515][Angew.Chem.,2017,vol.129,#13,p.3564-3569]

[15]Li,Weiyu;Xu,Hao;Zhou,Lei[OrganicandBiomolecularChemistry,2021,vol.19,#25,p.5649-5657]

[1]Stopka,Tobias;Marzo,Leyre;Zurro,Mercedes;Janich,Simon;Würthwein,Ernst-Ulrich;Daniliuc,ConstantinG.;Alemán,José;Mancheño,OlgaGarcía[AngewandteChemie-InternationalEdition,2015,vol.54,#17,p.5049-5053][Angew.Chem.,2015,vol.127,#17,p.5137-5141,5]

[2]Hogan,DavidT.;Dubrawski,Zachary;Gelfand,BenjaminS.;Sutherland,ToddC.[EuropeanJournalofOrganicChemistry,2022,vol.2022,#1]

[3]Tamano,Michiko;Koketsu,Jugo[BulletinoftheChemicalSocietyofJapan,1985,vol.58,#9,p.2577-2580]

[4]Hübner,Olaf;Himmel,Hans-Jörg;Kaifer,Elisabeth;Walter,Petra;Wild,Ute[Chemistry-AEuropeanJournal,2020,vol.26,#69,p.16504-16513]

[5]Charbit,JeanJacques;Galy,AnneMarie;Galy,JeanPierre;Barbe,Jacques[JournalofChemicalandEngineeringData,1989,vol.34,#1,p.136-137]

[6]Reed[JournaloftheChemicalSociety,1944,p.679]Bergmann;Fujise[JustusLiebigsAnnalenderChemie,1930,vol.483,p.65,76]

[7]Gini,Andrea;Uygur,Mustafa;Rigotti,Thomas;Alemán,José;GarcíaMancheño,Olga[Chemistry-AEuropeanJournal,2018,vol.24,#48,p.12509-12514]

[1]Surgi;Hodgeson[AnalyticalChemistry,1985,vol.57,#8,p.1737-1740]

[2]Koermendy[ActaChimicaAcademiaeScientiarumHungaricae,1959,vol.21,p.83,86vgl.EI312]

29897-82-3    26456-05-3    4217-54-3    719-54-0    100-52-7   
10-Methyl-9-pyrrolidin-1-yl-acridinium;perchlorate 

[1]BulletinoftheChemicalSocietyofJapan,1992,vol.65,p.55-60

[1]TetrahedronLetters,1990,vol.31,p.2869-2972

Literature

Title: 9-(3-Fluoro-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate monohydrate.

Journal: Acta crystallographica. Section E, Structure reports online 20120301

Title: 9-(2,5-Dimethyl-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.

Journal: Acta crystallographica. Section E, Structure reports online 20111201

Title: Chemiluminogenic features of 10-methyl-9-(phenoxycarbonyl)acridinium trifluoromethanesulfonates alkyl substituted at the benzene ring in aqueous media.

Journal: The Journal of organic chemistry 20110218

Title: Structure-activity relationship studies of acridones as potential antipsoriatic agents. 2. Synthesis and antiproliferative activity of 10-substituted hydroxy-10H-acridin-9-ones against human keratinocyte growth.

Journal: European journal of medicinal chemistry 20101101

Title: 9-(4-Fluoro-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: 9-(4-Chloro-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: 10-Methyl-9-[2-(propan-2-yl)phenoxy-carbonyl]-acridinium trifluoro-methane-sulfonate.

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: 9-Benzyl-10-methyl-acridinium trifluoro-methane-sulfonate.

Journal: Acta crystallographica. Section E, Structure reports online 20100701

Title: 9-(4-Methyl-phenoxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.

Journal: Acta crystallographica. Section E, Structure reports online 20100601

Title: 9-(4-Bromo-phenoxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.

Journal: Acta crystallographica. Section E, Structure reports online 20100601

Title: 10-Methyl-9-phenoxy-carbonyl-acridinium trifluoro-methane-sulfonate monohydrate.

Journal: Acta crystallographica. Section E, Structure reports online 20100401

Title: Ratiometric fluorescence response of N-methylacridone for methanesulfonic acid.

Journal: Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20050801

Title: Acridone derivatives are selective inhibitors of HIV-1 replication in chronically infected cells.

Journal: Antiviral research 19991001

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