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10201-71-5,MFCD07374874
Catalog No.:AA00068U

10201-71-5 | 2-Amino-3-methoxypyridine

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Purity
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1g
98%
in stock  
$12.00   $8.00
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5g
98%
in stock  
$15.00   $11.00
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10g
98%
in stock  
$28.00   $20.00
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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:
AA00068U
Chemical Name:
2-Amino-3-methoxypyridine
CAS Number:
10201-71-5
Molecular Formula:
C6H8N2O
Molecular Weight:
124.1405
MDL Number:
MFCD07374874
SMILES:
COc1cccnc1N
Properties
Properties
 
BP:
235°C at 760 mmHg  
Form:
Solid  
MP:
79-80°C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
87.1  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.5  

Upstream Synthesis Route

[1]Patent:US2013/210818,2013,A1,.Locationinpatent:Paragraph0380

[2]Patent:WO2009/115572,2009,A2,.Locationinpatent:Page/Pagecolumn114-115

[3]Patent:WO2014/206903,2014,A1,.Locationinpatent:Page/Pagecolumn15;16

[4]GreenChemistry,2017,vol.19,#3,p.809-815

[5]Patent:WO2013/92739,2013,A1,.Locationinpatent:Page/Pagecolumn16

[6]Patent:WO2010/96389,2010,A1,.Locationinpatent:Page/Pagecolumn45;48

[7]Patent:WO2010/135014,2010,A1,.Locationinpatent:Page/Pagecolumn53-55

[8]Patent:US2011/81316,2011,A1,.Locationinpatent:Page/Pagecolumn14

[9]Patent:US2009/22670,2009,A1,.Locationinpatent:Page/Pagecolumn19

[10]JournaloftheAmericanChemicalSociety,1947,vol.69,p.1147,1148

[11]RecueildesTravauxChimiquesdesPays-Bas,1955,vol.74,p.1171,1174

[12]AustralianJournalofChemistry,1995,vol.48,#5,p.1031-1038

[13]Patent:WO2010/100127,2010,A1,.Locationinpatent:Page/Pagecolumn71-72

[14]Patent:US9096593,2015,B2,.Locationinpatent:Page/Pagecolumn114

[15]ChemCatChem,2016,vol.8,#8,p.1485-1489

[16]EuropeanJournalofOrganicChemistry,2018,vol.2018,#2,p.209-214

[17]AppliedCatalysisA:General,2018,vol.559,p.127-137

[1]AdvancedSynthesisandCatalysis,2013,vol.355,#4,p.627-631

[2]JournalofMedicinalChemistry,1987,vol.30,#7,p.1150-1156

[3]Chemistry-AEuropeanJournal,2013,vol.19,#28,p.9137-9141

[1]JournalofMedicinalChemistry,1999,vol.42,#19,p.3934-3941

[1]Patent:US5972975,1999,A,

[1]RecueildesTravauxChimiquesdesPays-Bas,1955,vol.74,p.1171,1174

[2]JournaloftheAmericanChemicalSociety,1947,vol.69,p.1147,1148

Downstream Synthesis Route

[1]Patent:US2013/210818,2013,A1.Locationinpatent:Paragraph0380

[2]Patent:WO2009/115572,2009,A2.Locationinpatent:Page/Pagecolumn114-115

[3]Patent:WO2014/206903,2014,A1.Locationinpatent:Page/Pagecolumn15;16

[4]GreenChemistry,2017,vol.19,p.809-815

[5]ChemCatChem,2019,vol.11,p.4189-4195

[6]Patent:WO2013/92739,2013,A1.Locationinpatent:Page/Pagecolumn16

[7]Patent:WO2010/96389,2010,A1.Locationinpatent:Page/Pagecolumn45;48

[8]Patent:WO2010/135014,2010,A1.Locationinpatent:Page/Pagecolumn53-55

[9]Patent:US2011/81316,2011,A1.Locationinpatent:Page/Pagecolumn14

[10]Patent:US2009/22670,2009,A1.Locationinpatent:Page/Pagecolumn19

[11]JournaloftheAmericanChemicalSociety,1947,vol.69,p.1147,1148

[12]RecueildesTravauxChimiquesdesPays-Bas,1955,vol.74,p.1171,1174

[13]AustralianJournalofChemistry,1995,vol.48,p.1031-1038

[14]Patent:WO2010/100127,2010,A1.Locationinpatent:Page/Pagecolumn71-72

[15]Patent:US9096593,2015,B2.Locationinpatent:Page/Pagecolumn114

[16]ChemCatChem,2016,vol.8,p.1485-1489

[17]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.209-214

[18]AppliedCatalysisA:General,2018,vol.559,p.127-137

[1]TetrahedronLetters,1985,vol.26,p.2571-2574

[1]JournalofChemicalResearch,Miniprint,1986,p.670-688

[2]TetrahedronLetters,1985,vol.26,p.2571-2574

10201-71-5    1074-12-0   
C14H12N2O2 

[1]JournalofOrganicChemistry,1989,vol.54,p.5763-5768

10201-71-5   
(E)-1-(3-Benzyloxy-4-nitro-phenyl)-4-chloro-pent-1-en-3-one 
  128618-47-3 

[1]Chemicalandpharmaceuticalbulletin,1992,vol.40,p.1424-1438

Literature

Title: The hydrogen bonding and amino-imino tautomerization of the alkoxy-aminopyridines and amino-methoxypyrimidines with acetic acid The effects of the methoxy group.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20071101

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