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21260-41-3,MFCD01035882
Catalog No.:AA006XZG

21260-41-3 | 7-Hydroxy-2,3-dihydro-1h-cyclopenta[c]chromen-4-one

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250mg
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1g
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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:
AA006XZG
Chemical Name:
7-Hydroxy-2,3-dihydro-1h-cyclopenta[c]chromen-4-one
CAS Number:
21260-41-3
Molecular Formula:
C12H10O3
Molecular Weight:
202.2060
MDL Number:
MFCD01035882
SMILES:
Oc1ccc2c(c1)oc(=O)c1c2CCC1
Properties
Computed Properties
 
Complexity:
332  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
2  

Downstream Synthesis Route

[1]Locationinpatent:experimentalpartAzizian,Javad;Mohammadi,AliA.;Bidar,Ilyar;Mirzaei,Peiman[MonatsheftefurChemie,2008,vol.139,#7,p.805-808]

[2]Kumar,B.Sunil;Reddy,Y.Thirupathi;Reddy,P.Narsimha;Kumar;Rajitha[JournalofHeterocyclicChemistry,2006,vol.43,#2,p.477-479]

[3]SunilKumar;Kumar;Srinivasulu;Rajitha;ThirupathiReddy;NarsimhaReddy;Udupi[ChemistryofHeterocyclicCompounds,2006,vol.42,#2,p.172-175]

[4]Dabiri,Minoo;Salehi,Peyman;Zolfigol,MohammadAli;Baghbanzadeh,Mostafa[Heterocycles,2007,vol.71,#3,p.677-682]

[5]Abbasi,Zahra;Rezayati,Sobhan;Bagheri,Maryam;Hajinasiri,Rahimeh[ChineseChemicalLetters,2017,vol.28,#1,p.75-82]

[6]Khandekar;Khadilkar[Synlett,2002,#1,p.152-154]

[7]Dabiri,Minoo;Baghbanzadeh,Mostafa;Kiani,Shadi;Vakilzadeh,Yasamin[MonatsheftefurChemie,2007,vol.138,#10,p.997-999]

[8]Manhas,MagharS.;Ganguly,SubhenduN.;Mukherjee,Somdatta;Jain,AmitK.;Bose,AjayK.[TetrahedronLetters,2006,vol.47,#14,p.2423-2425]

[9]Locationinpatent:experimentalpartSoleimani,Ebrahim;Khodaei,MohammadMehdi;Batooie,Nasim;Samadi,Saadi[JournalofHeterocyclicChemistry,2012,vol.49,#2,p.409-412]

[10]Singh,PankajkumarR.;Singh,DevendrapratapU.;Samant,ShriniwasD.[Synlett,2004,#11,p.1909-1912]

[11]Veselovskaya;Shilin;Khilya[ChemistryofNaturalCompounds,2012,vol.48,#5,p.757-760][Khim.Prir.Soedin.,2012,vol.48,#5,p.679-681,3]

[12]Rahmatpour,Ali;Mohammadian,Sara[ComptesRendusChimie,2013,vol.16,#3,p.271-278]

[13]DallaVia,Lisa;Gia,Ornella;Viola,Giampietro;Bertoloni,Giulio;Santana,Lourdes;Uriarte,Eugenio[IlFarmaco,1998,vol.53,#10-11,p.638-644]

[14]Garazd;Garazd;Shilin;Panteleimonova;Khilya[ChemistryofNaturalCompounds,2002,vol.38,#3,p.230-242]

[15]Khomenko,Tatyana;Zakharenko,Alexandra;Odarchenko,Tatyana;Arabshahi,HomayonJohn;Sannikova,Victoriya;Zakharova,Olga;Korchagina,Dina;Reynisson,Jóhannes;Volcho,Konstantin;Salakhutdinov,Nariman;Lavrik,Olga[BioorganicandMedicinalChemistry,2016,vol.24,#21,p.5573-5581]

[16]Khomenko,TatyanaM.;Zarubaev,VladimirV.;Orshanskaya,IanaR.;Kadyrova,RenataA.;Sannikova,VictoriaA.;Korchagina,DinaV.;Volcho,KonstantinP.;Salakhutdinov,NarimanF.[BioorganicandMedicinalChemistryLetters,2017,vol.27,#13,p.2920-2925]

[17]Borisevich,SophiaS.;Galochkina,AnastasiaV.;Khomenko,TatyanaM.;Korchagina,DinaV.;Nikolaeva,YuliaV.;Petukhova,GalinaD.;Salakhutdinov,NarimanF.;Shtro,AnnaA.;Volcho,KonstantinP.[Molecules,2021,vol.26,#24]

[18]Ahmad;Desai[Proceedings-IndianAcademyofSciences,SectionA,1937,#5,p.277,282]

[19]Kozak,Witold;Dasko,Mateusz;Maslyk,Maciej;Pieczykolan,JerzyS.;Gielniewski,Bartlomiej;Rachon,Janusz;Demkowicz,Sebastian[RSCAdvances,2014,vol.4,#84,p.44350-44358]

[20]He,Qi;Liu,Jing;Lan,Jin-Shuai;Ding,Jiaoli;Sun,Yongbing;Fang,Yuanying;Jiang,Neng;Yang,Zunhua;Sun,Liyuan;Jin,Yi;Xie,Sai-Sai[BioorganicChemistry,2018,vol.81,p.512-528]

[1]Garazd;Garazd;Shilin;Panteleimonova;Khilya[ChemistryofNaturalCompounds,2002,vol.38,#3,p.230-242]

[1]Dubovik;Garazd;Vinogradova;Khilya[ChemistryofNaturalCompounds,2006,vol.42,#2,p.133-137]

[2]Veselovskaya;Shilin;Khilya[ChemistryofNaturalCompounds,2012,vol.48,#5,p.757-760][Khim.Prir.Soedin.,2012,vol.48,#5,p.679-681,3]

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.

Journal: Journal of medicinal chemistry 20081113

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Tags:21260-41-3 Molecular Formula|21260-41-3 MDL|21260-41-3 SMILES|21260-41-3 7-Hydroxy-2,3-dihydro-1h-cyclopenta[c]chromen-4-one