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Home Amines 21901-40-6
21901-40-6,MFCD00010692
Catalog No.:AA003GER

21901-40-6 | 2-Amino-4-methyl-5-nitropyridine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$6.00   $4.00
- +
5g
98%
in stock  
$7.00   $5.00
- +
10g
98%
in stock  
$9.00   $7.00
- +
25g
98%
in stock  
$22.00   $15.00
- +
100g
98%
in stock  
$42.00   $29.00
- +
  • 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:
AA003GER
Chemical Name:
2-Amino-4-methyl-5-nitropyridine
CAS Number:
21901-40-6
Molecular Formula:
C6H7N3O2
Molecular Weight:
153.1387
MDL Number:
MFCD00010692
SMILES:
[O-][N+](=O)c1cnc(cc1C)N
NSC Number:
52452
Properties
Properties
 
BP:
351.87 °C at 760 mmHg  
Form:
Solid  
MP:
223-225 °C(lit.)  
Refractive Index:
1.6500 (estimate)  
Solubility:
Soluble in DMSO.  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
156  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.7  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,1955,vol.20,p.1729,1731

[1]RussianJournalofOrganicChemistry,2009,vol.45,#1,p.115-118

[2]JournalofOrganicChemistry,1955,vol.20,p.1729,1731

[1]Patent:WO2005/97129,2005,A2,.Locationinpatent:Page/Pagecolumn176-177

[2]JournalofOrganicChemistry,1955,vol.20,p.1729,1731

[3]JournaloftheChemicalSociety,1954,p.2448,2455

[4]Patent:EP2366691,2011,A1,

[5]EuropeanJournalofMedicinalChemistry,2016,vol.121,p.143-157

[6]BioorganicandMedicinalChemistryLetters,2016,vol.26,#21,p.5229-5233

[7]ChemicalandPharmaceuticalBulletin,2017,vol.65,#1,p.66-81

[1]Patent:CN105906621,2016,A,.Locationinpatent:Paragraph0045

[2]Patent:EP2366691,2011,A1,.Locationinpatent:Page/Pagecolumn13

[3]JournaloftheChemicalSociety,1954,p.2448,2455

[4]JournalofOrganicChemistry,1955,vol.20,p.1729,1731

[5]Patent:WO2007/53394,2007,A1,.Locationinpatent:Page/Pagecolumn12

[6]EuropeanJournalofMedicinalChemistry,2016,vol.121,p.143-157

[7]BioorganicandMedicinalChemistryLetters,2016,vol.26,#21,p.5229-5233

[8]ChemicalandPharmaceuticalBulletin,2017,vol.65,#1,p.66-81

[1]Patent:EP2366691,2011,A1,.Locationinpatent:Page/Pagecolumn12-13

[2]Patent:CN105906621,2016,A,.Locationinpatent:Paragraph0044

[3]Patent:WO2005/97129,2005,A2,.Locationinpatent:Page/Pagecolumn176

[4]Patent:WO2012/103806,2012,A1,.Locationinpatent:Page/Pagecolumn43

Downstream Synthesis Route

[1]SpectrochimicaActaPartA:MolecularandBiomolecularSpectroscopy,2012,vol.96,p.952-962

[2]JournaloftheChemicalSociety,1954,p.2448,2455

[3]JournalofFluorineChemistry,2011,vol.132,p.541-547

[4]JournalofMolecularStructure,2013,vol.1043,p.15-27

[5]OrganicProcessResearchandDevelopment,2007,vol.11,p.885-888

[1]Patent:CN105906621,2016,A.Locationinpatent:Paragraph0045

[2]Patent:EP2366691,2011,A1.Locationinpatent:Page/Pagecolumn13

[3]JournaloftheChemicalSociety,1954,p.2448,2455

[4]Patent:WO2007/53394,2007,A1.Locationinpatent:Page/Pagecolumn12

[5]EuropeanJournalofMedicinalChemistry,2016,vol.121,p.143-157

[6]BioorganicandMedicinalChemistryLetters,2016,vol.26,p.5229-5233

[7]ChemicalandPharmaceuticalBulletin,2017,vol.65,p.66-81

[1]CurrentPatentAssignee:THEUNIVERSITYOFAUCKLAND-WO2022/64430,2022,A1Locationinpatent:Page/Pagecolumn131;132

[2]CurrentPatentAssignee:THEUNIVERSITYOFAUCKLAND-WO2022/64430,2022,A1Locationinpatent:Page/Pagecolumn131;132

[3]Gueiffier;Milhavet;Blache;Chavignon;Teulade;Madesclaire;Viols;Dauphin;Chapat[ChemicalandPharmaceuticalBulletin,1990,vol.38,#9,p.2352-2356]

[1]ActaChimicaHungarica,1986,vol.121,p.333-338

[2]ActaChimicaHungarica,1986,vol.121,p.333-338

[3]AustralianJournalofChemistry,1982,vol.35,p.2035-2040

[4]OrganicProcessResearchandDevelopment,2007,vol.11,p.885-888

[1]AustralianJournalofChemistry,1983,vol.36,p.1159-1166

Literature
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