Home Amines 6298-37-9
6298-37-9,MFCD00462821
Catalog No.:AA00348Y

6298-37-9 | 6-Aminoquinoxaline

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250mg
95%
in stock  
$6.00   $4.00
- +
1g
95%
in stock  
$7.00   $5.00
- +
5g
95%
in stock  
$23.00   $16.00
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25g
95%
in stock  
$44.00   $31.00
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100g
95%
in stock  
$173.00   $121.00
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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:
AA00348Y
Chemical Name:
6-Aminoquinoxaline
CAS Number:
6298-37-9
Molecular Formula:
C8H7N3
Molecular Weight:
145.1613
MDL Number:
MFCD00462821
SMILES:
Nc1ccc2c(c1)nccn2
NSC Number:
41810
Properties
Properties
 
BP:
331.3 °C at 760 mmHg  
Form:
Solid  
MP:
159 °C  
Refractive Index:
1.5400 (estimate)  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
137  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.9  

Upstream Synthesis Route

[1]Patent:US2012/178748,2012,A1,.Locationinpatent:Page/Pagecolumn43

[2]Patent:WO2013/6792,2013,A1,.Locationinpatent:Paragraph0170

[3]Patent:WO2005/42513,2005,A1,.Locationinpatent:Page/Pagecolumn71

[4]Heterocycles,2007,vol.72,p.353-361

[5]JournalofMedicinalChemistry,2016,vol.59,#13,p.6169-6186

[6]EuropeanJournalofOrganicChemistry,2005,#22,p.4870-4878

[7]TetrahedronLetters,2010,vol.51,#41,p.5402-5405

[8]Tetrahedron,1990,vol.46,#6,p.2089-2096

[9]BioorganicandMedicinalChemistry,2008,vol.16,#6,p.3255-3260

[10]JournaloftheAmericanChemicalSociety,1959,vol.81,p.6297,6300

[11]BioorganicandMedicinalChemistryLetters,2006,vol.16,#4,p.815-820

[12]Synthesis(Germany),2016,vol.48,#19,p.3232-3240

[1]OrganicLetters,2015,vol.17,#23,p.5934-5937

[2]AngewandteChemie-InternationalEdition,2015,vol.54,#12,p.3773-3777

[3]Angew.Chem.,2015,vol.127,#12,p.3844-3848,5

[4]AngewandteChemie-InternationalEdition,2015,vol.54,#12,p.3768-3772

[5]Angew.Chem.,2015,vol.127,#12,p.3839-3843,5

[6]OrganicLetters,2014,vol.16,#17,p.4388-4391

[1]Patent:US6323204,2001,B1,

[2]Patent:US5373010,1994,A,

[3]Patent:US5077292,1991,A,

[4]Patent:US5552403,1996,A,

[5]Patent:US5231096,1993,A,

[6]Patent:US5021416,1991,A,

[1]OrganicLetters,2017,vol.19,#11,p.2809-2812

[2]OrganicLetters,2013,vol.15,#14,p.3734-3737

[1]OrganicLetters,2017,vol.19,#11,p.2809-2812

Downstream Synthesis Route

[1]JournaloftheChemicalSociety,1953,p.2816,2819

[1]Patent:US2012/178748,2012,A1.Locationinpatent:Page/Pagecolumn43

[2]Patent:WO2013/6792,2013,A1.Locationinpatent:Paragraph0170

[3]Patent:WO2005/42513,2005,A1.Locationinpatent:Page/Pagecolumn71

[4]Heterocycles,2007,vol.72,p.353-361

[5]JournalofMedicinalChemistry,2016,vol.59,p.6169-6186

[6]EuropeanJournalofOrganicChemistry,2005,p.4870-4878

[7]TetrahedronLetters,2010,vol.51,p.5402-5405

[8]Tetrahedron,1990,vol.46,p.2089-2096

[9]BioorganicandMedicinalChemistry,2008,vol.16,p.3255-3260

[10]JournaloftheAmericanChemicalSociety,1959,vol.81,p.6297,6300

[11]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.815-820

[12]Synthesis,2016,vol.48,p.3232-3240

[1]Tetrahedron,1990,vol.46,p.2089-2096

[1]Tetrahedron,1990,vol.46,p.2089-2096

4363-93-3    6298-37-9   
quinolin-4-ylmethyl-quinoxalin-6-yl-amine 

[1]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.815-820

Literature

Title: 2,3-Substituted quinoxalin-6-amine analogs as antiproliferatives: a structure-activity relationship study.

Journal: Bioorganic & medicinal chemistry letters 20110401

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