Home Other Building Blocks 26452-98-2
26452-98-2,MFCD00053467
Catalog No.:AA002T7C

26452-98-2 | 1-Acetoxyindan

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1g
>98.0%(GC)
in stock  
$272.00   $190.00
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5g
>98.0%(GC)
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$875.00   $613.00
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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:
AA002T7C
Chemical Name:
1-Acetoxyindan
CAS Number:
26452-98-2
Molecular Formula:
C11H12O2
Molecular Weight:
176.2118
MDL Number:
MFCD00053467
SMILES:
CC(=O)OC1CCc2c1cccc2
Properties
Properties
 
BP:
255.8°C at 760 mmHg  

Computed Properties
 
Complexity:
200  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
1  
XLogP3:
2  

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1942,vol.64,p.912,914

[2]JournaloftheAmericanChemicalSociety,1942,vol.64,p.912,914

[3]ChemischeBerichte,1911,vol.44,p.1446

[1]Iwasaki,Takanori;Agura,Kazushi;Maegawa,Yusuke;Hayashi,Yukiko;Ohshima,Takashi;Mashima,Kazushi[Chemistry-AEuropeanJournal,2010,vol.16,#38,p.11567-11571]

[2]Whitmore;Gebhart[JournaloftheAmericanChemicalSociety,1942,vol.64,p.912,914]

[3]Battail,D.;Gagnaire,D.[BulletindelaSocieteChimiquedeFrance,1964,p.3076-3079]

[4]Brewster,J.H.;Buta,J.G.[JournaloftheAmericanChemicalSociety,1966,vol.88,#10,p.2233-2240]

[1]Xu,Wei;Xia,Wu;Guan,Yukun;Wang,Yiming;Lu,Cuifen;Yang,Guichun;Nie,Junqi;Chen,Zuxing[Reactiveandfunctionalpolymers,2016,vol.104,p.15-21]

[2]Locationinpatent:experimentalpartNiknam,Khodabakhsh;Saberi,Dariush[TetrahedronLetters,2009,vol.50,#37,p.5210-5214]

[3]Vuluga,Daniela;Legros,Julien;Crousse,Benoit;Bonnet-Delpon,Daniele[Chemistry-AEuropeanJournal,2010,vol.16,#6,p.1776-1779]

[4]Albadi,Jalal;Alihosseinzadeh,Amir;Mardani,Mehdi[ChineseJournalofCatalysis,2015,vol.36,#3,p.308-313]

[5]Locationinpatent:experimentalpartShirini,Farhad;Zolfigol,MohammadAli;Aliakbar,Ali-Reza;Albadi,Jalal[SyntheticCommunications,2010,vol.40,#7,p.1022-1028]

[6]DeMattos,MarcosCarlos;DeFonseca,ThiagoSousa;DaSilva,MarcosReinaldo;DeOliveira,MariaDaConceiçãoFerreira;DeLemos,TelmaLedaGomes;DeMarques,RicardoAraújo[AppliedCatalysisA:General,2015,vol.492,#1,p.76-82]

[7]Gavin,DeclanP.;Murphy,EdelJ.;Foley,AoifeM.;Castilla,IgnacioAbreu;Reen,F.Jerry;Woods,DavidF.;Collins,StuartG.;O'Gara,Fergal;Maguire,AnitaR.[AdvancedSynthesisandCatalysis,2019,vol.361,#11,p.2466-2474]

[8]Hueckeletal.[JustusLiebigsAnnalenderChemie,1935,vol.518,p.155,173,175][JustusLiebigsAnnalenderChemie,1938,vol.533,p.128,170]

[9]Weissgerber[ChemischeBerichte,1911,vol.44,p.1446]

[10]Bakker;Spruijt;VanRantwijk;Sheldon[TetrahedronAsymmetry,2000,vol.11,#8,p.1801-1808]

[11]Joly;Nair,MangalamS.[TetrahedronAsymmetry,2001,vol.12,#16,p.2283-2287]

[12]Ghanem,Ashraf;Schurig,Volker[TetrahedronAsymmetry,2003,vol.14,#17,p.2547-2555]

[13]Powell,DavidA.;Pelletier,Guillaume[TetrahedronLetters,2008,vol.49,#16,p.2495-2498]

[14]Locationinpatent:experimentalpartTaghavi,S.Abdolmanaf;Moghadam,Majid;Mohammadpoor-Baltork,Iraj;Tangestaninejad,Shahram;Mirkhani,Valiollah;Khosropour,AhmadReza[InorganicaChimicaActa,2011,vol.377,#1,p.159-164]

[15]Locationinpatent:experimentalpartMerabet-Khelassi,Mounia;Houiene,Zahia;Aribi-Zouioueche,Louisa;Riant,Olivier[TetrahedronAsymmetry,2012,vol.23,#11-12,p.828-833]

[16]Houiene,Zahia;Merabet-Khelassi,Mounia;Bouzemi,Nassima;Riant,Olivier;Aribi-Zouioueche,Louisa[TetrahedronAsymmetry,2013,vol.24,#5-6,p.290-296]

[17]Zadi,Amna;Merabet-Khelassi,Mounia;Aribi-Zouioueche,Louisa[CatalysisLetters,2015,vol.145,#4,p.1054-1061]

[1]JournaloftheChemicalSociety.Chemicalcommunications,1988,p.598-600

[2]TetrahedronLetters,1998,vol.39,p.8881-8884

[1]Locationinpatent:schemeortableFarhadi,Saeid;Panahandehjoo,Somayeh[AppliedCatalysisA:General,2010,vol.382,#2,p.293-302]

[2]CurrentPatentAssignee:UNIVERSITYOFSYDNEY-US2010/81849,2010,A1Locationinpatent:Page/Pagecolumn5;19

[3]Pincock,J.A.;Wedge,P.J.[JournalofOrganicChemistry,1995,vol.60,#13,p.4067-4076]

Literature

Title: Indanylacetic acids as PPAR-delta activator insulin sensitizers.

Journal: Bioorganic & medicinal chemistry letters 20070801

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