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6480-68-8,MFCD00006770
Catalog No.:AA0035RX

6480-68-8 | Quinoline-3-carboxylic acid

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Purity
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1g
98%
in stock  
$6.00   $4.00
- +
5g
98%
in stock  
$16.00   $11.00
- +
10g
98%
in stock  
$28.00   $20.00
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25g
98%
in stock  
$60.00   $42.00
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100g
98%
in stock  
$232.00   $163.00
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  • 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:
AA0035RX
Chemical Name:
Quinoline-3-carboxylic acid
CAS Number:
6480-68-8
Molecular Formula:
C10H7NO2
Molecular Weight:
173.1681
MDL Number:
MFCD00006770
SMILES:
OC(=O)c1cnc2c(c1)cccc2
NSC Number:
403263
Properties
Properties
 
BP:
348.7°C at 760 mmHg  
Form:
Solid  
MP:
277-280 °C(lit.)  
Refractive Index:
1.5200 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
205  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
1.7  

Upstream Synthesis Route

[1]Patent:WO2014/33604,2014,A1,.Locationinpatent:Page/Pagecolumn48

[2]OrganicandBiomolecularChemistry,2016,vol.14,#24,p.5505-5510

[3]TetrahedronAsymmetry,2013,vol.24,#18,p.1142-1147

[4]Patent:US2016/122303,2016,A1,.Locationinpatent:Paragraph0078

[5]TetrahedronAsymmetry,2010,vol.21,#18,p.2307-2313

[6]JournalofMedicinalChemistry,2010,vol.53,#3,p.1281-1287

[7]EuropeanJournalofMedicinalChemistry,2018,vol.149,p.56-68

[8]BioorganicandMedicinalChemistry,2004,vol.12,#15,p.4179-4188

[9]Patent:CN107383024,2017,A,.Locationinpatent:Paragraph0377

[10]Patent:WO2018/152107,2018,A1,.Locationinpatent:Page/Pagecolumn19

[11]JournalofMedicinalChemistry,1982,vol.25,#9,p.1081-1091

[12]JournalofOrganicChemistry,1945,vol.10,p.76,85

[13]CanadianJournalofChemistry,1984,vol.62,p.1301-1307

[14]Phytochemistry(Elsevier),1984,vol.23,#6,p.1225-1228

[15]Patent:WO2017/11323,2017,A1,.Locationinpatent:Paragraph00343

[1]Patent:US2003/69284,2003,A1,

[2]Tetrahedron,2015,vol.71,#10,p.1588-1596

[3]OrganicLetters,2018,

[1]JustusLiebigsAnnalenderChemie,1936,vol.526,p.22,33

[1]AdvancedSynthesisandCatalysis,2010,vol.352,#13,p.2166-2170

[2]JournalofOrganicChemistry,1999,vol.64,#6,p.1823-1830

[3]Patent:WO2012/178015,2012,A2,

[1]JournalofChemicalResearch,Miniprint,1991,#5,p.914-934

Downstream Synthesis Route

[1]JustusLiebigsAnnalenderChemie,1936,vol.526,p.22,33

[2]OrganicLetters,2019,vol.21,p.2464-2467

[1]TetrahedronLetters,1995,vol.36,p.9561-9564

[2]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.1099-1104

[3]JournaloftheAmericanChemicalSociety,1941,vol.63,p.1553,1554

[4]JournaloftheAmericanChemicalSociety,1941,vol.63,p.1553,1554

[5]BulletinoftheChemicalSocietyofJapan,1987,vol.60,p.2891-2898

[6]MagneticResonanceinChemistry,2019,vol.57,p.331-341

[1]Patent:WO2014/33604,2014,A1.Locationinpatent:Page/Pagecolumn48

[2]OrganicandBiomolecularChemistry,2016,vol.14,p.5505-5510

[3]Patent:WO2020/28482,2020,A1.Locationinpatent:Paragraph00134

[4]TetrahedronAsymmetry,2013,vol.24,p.1142-1147

[5]Patent:US2016/122303,2016,A1.Locationinpatent:Paragraph0078

[6]TetrahedronAsymmetry,2010,vol.21,p.2307-2313

[7]JournalofMedicinalChemistry,2010,vol.53,p.1281-1287

[8]EuropeanJournalofMedicinalChemistry,2018,vol.149,p.56-68

[9]BioorganicandMedicinalChemistry,2004,vol.12,p.4179-4188

[10]Patent:CN107383024,2017,A.Locationinpatent:Paragraph0377

[11]Patent:WO2018/152107,2018,A1.Locationinpatent:Page/Pagecolumn19

[12]JournalofMedicinalChemistry,1982,vol.25,p.1081-1091

[13]JournalofOrganicChemistry,1945,vol.10,p.76,85

[14]CanadianJournalofChemistry,1984,vol.62,p.1301-1307

[15]Phytochemistry,1984,vol.23,p.1225-1228

[16]Patent:WO2017/11323,2017,A1.Locationinpatent:Paragraph00343

[1]JournaloftheAmericanChemicalSociety,1941,vol.63,p.1553,1554

[2]Patent:WO2016/8411,2016,A1.Locationinpatent:Paragraph0143

[3]MagneticResonanceinChemistry,2019,vol.57,p.331-341

Literature

Title: Temperature-/solvent-dependent low-dimensional compounds based on quinoline-2,3-dicarboxylic acid: structures and fluorescent properties.

Journal: Dalton transactions (Cambridge, England : 2003) 20121014

Title: catena-Poly[disilver(I)(Ag-Ag)-bis-(μ(3)-quinoline-3-carboxyl-ato)-1:2:1'κ(3)O:O':N;2:1'':2''κ(3)N:O:O'].

Journal: Acta crystallographica. Section E, Structure reports online 20120901

Title: Poly[(μ(2)-quinoline-3-carboxyl-ato-κN:O)(μ(2)-quinoline-3-carboxyl-ato-κN:O,O')cadmium].

Journal: Acta crystallographica. Section E, Structure reports online 20120201

Title: catena-Poly[[diaqua-strontium]-bis-(μ-quinoline-3-carboxyl-ato)].

Journal: Acta crystallographica. Section E, Structure reports online 20111001

Title: 6-Chloro-2-cyclo-propyl-4-(trifluoro-meth-yl)quinoline.

Journal: Acta crystallographica. Section E, Structure reports online 20110301

Title: catena-Poly[[diaqua-calcium(II)]-bis-(μ-quinoline-3-carboxyl-ato)].

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

Title: Controlled release of active as a consequence of the die diameter in solid lipid extrusion.

Journal: Journal of controlled release : official journal of the Controlled Release Society 20081124

Title: Small-molecule inhibitors of histone acetyltransferase activity: identification and biological properties.

Journal: Journal of medicinal chemistry 20061116

Title: Synthesis and antiproliferative evaluation of certain pyrido[3,2-g]quinoline derivatives.

Journal: Bioorganic & medicinal chemistry 20061115

Title: Simultaneous determination of niacin, niacinamide and nicotinuric acid in human plasma.

Journal: Journal of pharmaceutical and biomedical analysis 20050104

Title: Synthesis and antimycobacterial activities of ring-substituted quinolinecarboxylic acid/ester analogues. Part 1.

Journal: Bioorganic & medicinal chemistry 20040801

Title: Transformation of cinoxacin by Beauveria bassiana.

Journal: FEMS microbiology letters 20020827

Title: A molybdenum-containing dehydrogenase catalyzing an unusual 2-hydroxylation of nicotinic acid.

Journal: Applied microbiology and biotechnology 20020401

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