15450-76-7,MFCD00216696
Catalog No.:AA0032ZL

15450-76-7 | Quinoline-2,8-diol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
95%
in stock  
$12.00   $9.00
- +
25g
98%
in stock  
$50.00   $35.00
- +
100g
95%
in stock  
$112.00   $79.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0032ZL
Chemical Name:
Quinoline-2,8-diol
CAS Number:
15450-76-7
Molecular Formula:
C9H7NO2
Molecular Weight:
161.1574
MDL Number:
MFCD00216696
SMILES:
Oc1ccc2c(n1)c(O)ccc2
NSC Number:
108383
Properties
Properties
 
BP:
403.2°C at 760 mmHg  
Form:
Solid  
MP:
-290 °C (dec.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
225  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1  

Upstream Synthesis Route

[1]CanadianJournalofChemistry,2005,vol.83,#5,p.460-470

[1]CanadianJournalofChemistry,2005,vol.83,#5,p.460-470

[2]JournalofFluorescence,2018,vol.28,#5,p.1121-1126

[1]MonatsheftefuerChemie,1895,vol.16,p.761

[2]ChemistryandIndustry(London,UnitedKingdom),1957,p.1271

[1]YakugakuZasshi,1951,vol.71,p.784

[2]Chem.Abstr.,1952,p.4007

[3]YakugakuZasshi,1958,vol.78,p.697,698

[4]Chem.Abstr.,1958,p.18406

[1]Patent:EP2634177,2013,A1,.Locationinpatent:Paragraph0217;0218

[2]EuropeanJournalofMedicinalChemistry,2018,vol.156,p.790-799

[3]CanadianJournalofChemistry,2005,vol.83,#5,p.460-470

[4]Patent:WO2004/35549,2004,A1,.Locationinpatent:Page71

[5]Patent:WO2014/100730,2014,A1,.Locationinpatent:Paragraph00314

[6]JournalofFluorescence,2018,vol.28,#5,p.1121-1126

Downstream Synthesis Route

[1]JournalofOrganicChemistry,2010,vol.75,p.424-433

[2]MonatsheftefurChemie,1895,vol.16,p.761

[3]MonatsheftefurChemie,1895,vol.16,p.761

[4]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1951,vol.71,p.784    Chem.Abstr.,1952,p.4007

[5]Patent:CN108947898,2018,A.Locationinpatent:Paragraph0058-0060

[6]BioorganicandMedicinalChemistryLetters,2019,vol.29,p.749-754

15450-76-7    98-88-4   
8-benzoyloxy-quinolin-2-ol 

[1]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

[2]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1958,vol.78,p.697,698    Chem.Abstr.,1958,p.18406

15450-76-7    98-88-4   
2,8-bis-benzoyloxy-quinoline 

[1]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1951,vol.71,p.784    Chem.Abstr.,1952,p.4007

[1]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

[2]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

Literature

Title: Quinoline biodegradation and its nitrogen transformation pathway by a Pseudomonas sp. strain.

Journal: Biodegradation 20100601

Title: Interaction of 8-hydroxyquinoline with soil environment mediates its ecological function.

Journal: PloS one 20100101

Title: Aerobic biodegradation characteristics and metabolic products of quinoline by a Pseudomonas strain.

Journal: Bioresource technology 20091101

Title: [Isolation, identification, and biodegradation characteristics of a quinoline-degrading bacterium].

Journal: Huan jing ke xue= Huanjing kexue 20081201

Title: A new Hg(2+) -selective fluorescent sensor based on a 1,3-alternate thiacalix[4]arene anchored with four 8-quinolinoloxy groups.

Journal: Inorganic chemistry 20070806

Title: Configuration-specific synthesis of the facial and meridional isomers of tris(8-hydroxyquinolinate)aluminum (Alq3).

Journal: Inorganic chemistry 20060724

Title: Antioxidant effects of quinoline alkaloids and 2,4-di-tert-butylphenol isolated from Scolopendra subspinipes.

Journal: Biological & pharmaceutical bulletin 20060401

Title: Prediction of genotoxicity of chemical compounds by statistical learning methods.

Journal: Chemical research in toxicology 20050601

Title: 2-Oxoquinoline 8-monooxygenase oxygenase component: active site modulation by Rieske-[2Fe-2S] center oxidation/reduction.

Journal: Structure (London, England : 1993) 20050501

Title: Antimicrosporidial activity of (fluoro)quinolones in vitro and in vivo.

Journal: Folia parasitologica 20050501

Title: Conversion of tris(8-quinolinolato-N1, O8) aluminum to 8-hydroxyquinoline and activity in bacterial reverse mutation assays.

Journal: Mutation research 20050404

Quotation Request
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Additional Info:
SDS
Historical Records
Tags:15450-76-7 Molecular Formula|15450-76-7 MDL|15450-76-7 SMILES|15450-76-7 Quinoline-2,8-diol
Catalog No.: AA0032ZL
15450-76-7,MFCD00216696
15450-76-7 | Quinoline-2,8-diol
Pack Size: 5g
Purity: 95%
in stock
$12.00 $9.00
Pack Size: 25g
Purity: 98%
in stock
$50.00 $35.00
Pack Size: 100g
Purity: 95%
in stock
$112.00 $79.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0032ZL
Chemical Name: Quinoline-2,8-diol
CAS Number: 15450-76-7
Molecular Formula: C9H7NO2
Molecular Weight: 161.1574
MDL Number: MFCD00216696
SMILES: Oc1ccc2c(n1)c(O)ccc2
NSC Number: 108383
Properties
BP: 403.2°C at 760 mmHg  
Form: Solid  
MP: -290 °C (dec.)  
Storage: Keep in dry area;Room Temperature;  
Complexity: 225  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1  
Upstream Synthesis Route
15450-72-3    15450-76-7 

[1]CanadianJournalofChemistry,2005,vol.83,#5,p.460-470

1127-45-3    15450-76-7 

[1]CanadianJournalofChemistry,2005,vol.83,#5,p.460-470

[2]JournalofFluorescence,2018,vol.28,#5,p.1121-1126

148-24-3    15450-76-7 

[1]MonatsheftefuerChemie,1895,vol.16,p.761

[2]ChemistryandIndustry(London,UnitedKingdom),1957,p.1271

84-88-8    15450-76-7 

[1]YakugakuZasshi,1951,vol.71,p.784

[2]Chem.Abstr.,1952,p.4007

[3]YakugakuZasshi,1958,vol.78,p.697,698

[4]Chem.Abstr.,1958,p.18406

15450-76-7    31568-91-9 

[1]Patent:EP2634177,2013,A1,.Locationinpatent:Paragraph0217;0218

[2]EuropeanJournalofMedicinalChemistry,2018,vol.156,p.790-799

[3]CanadianJournalofChemistry,2005,vol.83,#5,p.460-470

[4]Patent:WO2004/35549,2004,A1,.Locationinpatent:Page71

[5]Patent:WO2014/100730,2014,A1,.Locationinpatent:Paragraph00314

[6]JournalofFluorescence,2018,vol.28,#5,p.1121-1126

Downstream Synthesis Route
15450-76-7    108-24-7    15450-72-3 

[1]JournalofOrganicChemistry,2010,vol.75,p.424-433

[2]MonatsheftefurChemie,1895,vol.16,p.761

[3]MonatsheftefurChemie,1895,vol.16,p.761

[4]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1951,vol.71,p.784    Chem.Abstr.,1952,p.4007

[5]Patent:CN108947898,2018,A.Locationinpatent:Paragraph0058-0060

[6]BioorganicandMedicinalChemistryLetters,2019,vol.29,p.749-754

15450-76-7    98-88-4   
8-benzoyloxy-quinolin-2-ol 

[1]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

[2]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1958,vol.78,p.697,698    Chem.Abstr.,1958,p.18406

15450-76-7    98-88-4   
2,8-bis-benzoyloxy-quinoline 

[1]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

15450-76-7    77-78-1    42521-90-4 

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1951,vol.71,p.784    Chem.Abstr.,1952,p.4007

15450-76-7    52749-50-5 

[1]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

[2]JournaloftheAmericanChemicalSociety,1944,vol.66,p.1166,1168

Literature fold

Title: Quinoline biodegradation and its nitrogen transformation pathway by a Pseudomonas sp. strain.

Journal: Biodegradation20100601

Title: Interaction of 8-hydroxyquinoline with soil environment mediates its ecological function.

Journal: PloS one20100101

Title: Aerobic biodegradation characteristics and metabolic products of quinoline by a Pseudomonas strain.

Journal: Bioresource technology20091101

Title: [Isolation, identification, and biodegradation characteristics of a quinoline-degrading bacterium].

Journal: Huan jing ke xue= Huanjing kexue20081201

Title: A new Hg(2+) -selective fluorescent sensor based on a 1,3-alternate thiacalix[4]arene anchored with four 8-quinolinoloxy groups.

Journal: Inorganic chemistry20070806

Title: Configuration-specific synthesis of the facial and meridional isomers of tris(8-hydroxyquinolinate)aluminum (Alq3).

Journal: Inorganic chemistry20060724

Title: Antioxidant effects of quinoline alkaloids and 2,4-di-tert-butylphenol isolated from Scolopendra subspinipes.

Journal: Biological & pharmaceutical bulletin20060401

Title: Prediction of genotoxicity of chemical compounds by statistical learning methods.

Journal: Chemical research in toxicology20050601

Title: 2-Oxoquinoline 8-monooxygenase oxygenase component: active site modulation by Rieske-[2Fe-2S] center oxidation/reduction.

Journal: Structure (London, England : 1993)20050501

Title: Antimicrosporidial activity of (fluoro)quinolones in vitro and in vivo.

Journal: Folia parasitologica20050501

Title: Conversion of tris(8-quinolinolato-N1, O8) aluminum to 8-hydroxyquinoline and activity in bacterial reverse mutation assays.

Journal: Mutation research20050404

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