Home Nitro Compounds 22246-16-8
22246-16-8,MFCD00559317
Catalog No.:AA003N8H

22246-16-8 | 6-Nitro-3,4-dihydroquinolin-2(1H)-one

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$24.00   $17.00
- +
5g
95%
in stock  
$80.00   $56.00
- +
10g
95%
in stock  
$127.00   $89.00
- +
25g
95%
in stock  
$270.00   $189.00
- +
100g
95%
in stock  
$620.00   $434.00
- +
  • 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:
AA003N8H
Chemical Name:
6-Nitro-3,4-dihydroquinolin-2(1H)-one
CAS Number:
22246-16-8
Molecular Formula:
C9H8N2O3
Molecular Weight:
192.1714
MDL Number:
MFCD00559317
SMILES:
O=C1CCc2c(N1)ccc(c2)[N+](=O)[O-]
Properties
Properties
 
BP:
420.3°C at 760 mmHg  
Form:
Solid  
MP:
201-202 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
261  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.9  

Upstream Synthesis Route

[1]Patent:WO2015/38417,2015,A1,.Locationinpatent:Page/Pagecolumn90;91

[2]BioorganicandMedicinalChemistryLetters,2008,vol.18,#16,p.4606-4609

[3]Patent:WO2006/71940,2006,A2,.Locationinpatent:Page/Pagecolumn416

[4]ProceedingsoftheImperialAcademy(Tokyo),1939,vol.15,p.148,153

[5]Chem.Zentralbl.,1939,vol.110,#II,p.3089

[6]ArchivderPharmazie,2008,vol.341,#12,p.794-799

[7]EuropeanJournalofMedicinalChemistry,2014,vol.73,p.217-224

[8]Patent:WO2016/33100,2016,A1,.Locationinpatent:Page/Pagecolumn145

[9]EuropeanJournalofMedicinalChemistry,2018,vol.151,p.450-461

[10]Patent:WO2018/112037,2018,A1,.Locationinpatent:Paragraph0146

[1]Heterocycles,1998,vol.48,#12,p.2637-2641

[2]Patent:US2007/27184,2007,A1,.Locationinpatent:Page/Pagecolumn18;25

[3]BioorganicandMedicinalChemistryLetters,2006,vol.16,#20,p.5270-5274

[4]Patent:KR101576386,2015,B1,.Locationinpatent:Paragraph0190;0193-0194

[1]BioorganicandMedicinalChemistryLetters,2008,vol.18,#16,p.4606-4609

[2]Patent:US2007/27184,2007,A1,.Locationinpatent:Page/Pagecolumn18;25

[3]Patent:WO2006/71940,2006,A2,.Locationinpatent:Page/Pagecolumn416

[4]Patent:US2008/234237,2008,A1,.Locationinpatent:Page/Pagecolumn35

[5]Patent:WO2003/72553,2003,A1,.Locationinpatent:Page/Pagecolumn150

[6]Patent:US2004/147760,2004,A1,.Locationinpatent:Page73

[7]Patent:US2018/199575,2018,A1,.Locationinpatent:Paragraph0153-0154

[8]Patent:US2017/27172,2017,A1,.Locationinpatent:Paragraph0187;0173;0174;0181;0183;0189

[9]Patent:WO2015/38417,2015,A1,.Locationinpatent:Page/Pagecolumn90

[10]JournaloftheAmericanChemicalSociety,2014,vol.136,#38,p.13277-13282

[11]ProceedingsoftheImperialAcademy(Tokyo),1939,vol.15,p.148,153

[12]Chem.Zentralbl.,1939,vol.110,#II,p.3089

[13]Patent:US2003/195201,2003,A1,

[14]ArchivderPharmazie,2008,vol.341,#12,p.794-799

[15]Patent:WO2013/159095,2013,A1,.Locationinpatent:Paragraph0082

[16]EuropeanJournalofMedicinalChemistry,2014,vol.73,p.217-224

[17]Patent:KR101576386,2015,B1,.Locationinpatent:Paragraph0190-0192

[1]Heterocycles,1998,vol.48,#12,p.2637-2641

[1]JournaloftheAmericanChemicalSociety,2014,vol.136,#38,p.13277-13282

[2]Patent:WO2015/38417,2015,A1,

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.4606-4609

[2]Patent:US2007/27184,2007,A1.Locationinpatent:Page/Pagecolumn18;25

[3]Patent:WO2006/71940,2006,A2.Locationinpatent:Page/Pagecolumn416

[4]Patent:US2008/234237,2008,A1.Locationinpatent:Page/Pagecolumn35

[5]Patent:WO2003/72553,2003,A1.Locationinpatent:Page/Pagecolumn150

[6]Patent:US2004/147760,2004,A1.Locationinpatent:Page73

[7]Patent:US2018/199575,2018,A1.Locationinpatent:Paragraph0153-0154

[8]Patent:US2017/27172,2017,A1.Locationinpatent:Paragraph0187;0173;0174;0181;0183;0189

[9]Patent:WO2015/38417,2015,A1.Locationinpatent:Page/Pagecolumn90

[10]JournaloftheAmericanChemicalSociety,2014,vol.136,p.13277-13282

[11]ProceedingsoftheImperialAcademy(Tokyo),1939,vol.15,p.148,153    ChemischesZentralblatt,1939,vol.110,p.3089

[12]Patent:US2003/195201,2003,A1

[13]ArchivderPharmazie,2008,vol.341,p.794-799

[14]Patent:WO2013/159095,2013,A1.Locationinpatent:Paragraph0082

[15]EuropeanJournalofMedicinalChemistry,2014,vol.73,p.217-224

[16]Patent:KR101576386,2015,B1.Locationinpatent:Paragraph0190-0192

[17]Patent:CN109810054,2019,A.Locationinpatent:Paragraph0009;0010

[1]Patent:WO2020/28461,2020,A1.Locationinpatent:Paragraph00177-

[2]Patent:WO2015/38417,2015,A1.Locationinpatent:Page/Pagecolumn90;91

[3]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.4606-4609

[4]Patent:WO2006/71940,2006,A2.Locationinpatent:Page/Pagecolumn416

[5]ProceedingsoftheImperialAcademy(Tokyo),1939,vol.15,p.148,153    ChemischesZentralblatt,1939,vol.110,p.3089

[6]ArchivderPharmazie,2008,vol.341,p.794-799

[7]EuropeanJournalofMedicinalChemistry,2014,vol.73,p.217-224

[8]Patent:WO2016/33100,2016,A1.Locationinpatent:Page/Pagecolumn145

[9]EuropeanJournalofMedicinalChemistry,2018,vol.151,p.450-461

[10]Patent:WO2018/112037,2018,A1.Locationinpatent:Paragraph0146

[11]Patent:CN109810054,2019,A.Locationinpatent:Paragraph0009;0010

[1]ProceedingsoftheImperialAcademy(Tokyo),1939,vol.15,p.148,153    ChemischesZentralblatt,1939,vol.110,p.3089

22246-16-8   
<i>N</i>2-methyl-quinoline-2,6-diamine 

[1]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.5270-5274

22246-16-8   
N2,N2-dimethylquinoline-2,6-diamine 

[1]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.5270-5274

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Tags:22246-16-8 Molecular Formula|22246-16-8 MDL|22246-16-8 SMILES|22246-16-8 6-Nitro-3,4-dihydroquinolin-2(1H)-one