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26892-90-0,MFCD00173406
Catalog No.:AA003LH5

26892-90-0 | 4-Hydroxyquinoline-3-carboxylic acid ethyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$11.00   $8.00
- +
5g
98%
in stock  
$31.00   $22.00
- +
25g
98%
in stock  
$94.00   $66.00
- +
500g
98%
in stock  
$1,758.00   $1,231.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003LH5
Chemical Name:
4-Hydroxyquinoline-3-carboxylic acid ethyl ester
CAS Number:
26892-90-0
Molecular Formula:
C12H11NO3
Molecular Weight:
217.2206
MDL Number:
MFCD00173406
SMILES:
CCOC(=O)c1c[nH]c2c(c1=O)cccc2
NSC Number:
4345
Properties
Properties
 
BP:
343.7°C at 760 mmHg  
Form:
Solid  
MP:
271 - 273 °C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
335  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2  

Upstream Synthesis Route

[1]MolecularCrystalsandLiquidCrystalsScienceandTechnologySectionA:MolecularCrystalsandLiquidCrystals,2000,vol.344,p.163-168

[2]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1995,vol.31,#2,p.167-175

[3]KhimiyaGeterotsiklicheskikhSoedinenii,1995,#2,p.195-203

[4]Patent:CN106187887,2016,A,.Locationinpatent:Paragraph0015;0048;0049;0050;0051;0052;0053

[5]JournaloftheAmericanChemicalSociety,1946,vol.68,p.1264

[6]JournaloftheChemicalSociety,1948,p.893

[7]JournaloftheChemicalSociety,1946,p.1033,1035

[8]BioorganicandMedicinalChemistry,2009,vol.17,#5,p.1948-1956

[9]EuropeanJournalofMedicinalChemistry,2010,vol.45,#5,p.1821-1827

[1]Patent:US2011/98311,2011,A1,

[1]Patent:US4079058,1978,A,

[2]Patent:US2008/90864,2008,A1,.Locationinpatent:Page/Pagecolumn7

[3]Patent:WO2007/79139,2007,A2,.Locationinpatent:Page/Pagecolumn46

[4]EuropeanJournalofMedicinalChemistry,2015,vol.103,p.1-16

[5]MolecularCrystalsandLiquidCrystalsScienceandTechnologySectionA:MolecularCrystalsandLiquidCrystals,2000,vol.344,p.163-168

[6]JournaloftheAmericanChemicalSociety,1939,vol.61,p.2890,2893

[7]BioorganicandMedicinalChemistryLetters,2005,vol.15,#12,p.2980-2985

[8]JournalofMedicinalChemistry,2006,vol.49,#21,p.6351-6363

[9]Patent:US2008/306048,2008,A1,.Locationinpatent:Page/Pagecolumn17

[10]BioorganicandMedicinalChemistry,2009,vol.17,#5,p.1948-1956

[11]BioorganicandMedicinalChemistryLetters,2010,vol.20,#2,p.689-693

[12]Patent:US2012/309758,2012,A1,.Locationinpatent:Page/Pagecolumn60

[13]Patent:US2015/231142,2015,A1,.Locationinpatent:Paragraph0351

[14]Patent:WO2018/64632,2018,A1,.Locationinpatent:Paragraph00213;00214

[15]Patent:WO2018/107100,2018,A1,.Locationinpatent:Paragraph00232;00233

[16]Patent:US2018/280349,2018,A1,.Locationinpatent:Paragraph0096

[1]Patent:CN108623581,2018,A,.Locationinpatent:Page/Pagecolumn6

[2]Patent:CN108623561,2018,A,.Locationinpatent:Paragraph0014

[3]Patent:CN108690024,2018,A,.Locationinpatent:Paragraph0144

[4]Patent:CN108623562,2018,A,.Locationinpatent:Paragraph0067

[5]Patent:CN108623560,2018,A,.Locationinpatent:Page/Pagecolumn36

[6]Patent:WO2005/123686,2005,A1,.Locationinpatent:Page/Pagecolumn75-76

[7]JournalofMedicinalChemistry,1993,vol.36,#11,p.1669-1673

[8]BioorganicandMedicinalChemistryLetters,2003,vol.13,#8,p.1487-1490

[9]EuropeanJournalofMedicinalChemistry,2010,vol.45,#5,p.1821-1827

[10]Patent:US2012/309758,2012,A1,

[11]Patent:WO2018/107100,2018,A1,

[12]Patent:US2018/280349,2018,A1,

[1]Patent:CN106187887,2016,A,.Locationinpatent:Paragraph0015;0063;0064;0065;0046;0047

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1946,vol.68,p.1264

[1]JournaloftheAmericanChemicalSociety,1954,vol.76,p.2760

[2]JournaloftheChemicalSociety,1946,p.1035

26892-90-0    141-43-5   
4-hydroxy-quinoline-3-carboxylicacid-(2-hydroxy-ethylamide) 

[1]JournaloftheAmericanChemicalSociety,1947,vol.69,p.200,203

26892-90-0    62-53-3   
4-hydroxy-quinoline-3-carboxylicacidanilide 

[1]JournaloftheChemicalSociety,1950,p.607,609

[1]AustralianJournalofScientificResearch,SeriesA:PhysicalSciences,1949,vol.<A>2,p.630,634

Literature
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SDS
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