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4021-07-2,MFCD00191553
Catalog No.:AA0033OS

4021-07-2 | 3-Methylpicolinic acid

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5g
97%
in stock  
$8.00   $6.00
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10g
97%
in stock  
$12.00   $8.00
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100g
97%
in stock  
$57.00   $40.00
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500g
97%
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$284.00   $199.00
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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:
AA0033OS
Chemical Name:
3-Methylpicolinic acid
CAS Number:
4021-07-2
Molecular Formula:
C7H7NO2
Molecular Weight:
137.1360
MDL Number:
MFCD00191553
SMILES:
OC(=O)c1ncccc1C
NSC Number:
109145
Properties
Properties
 
BP:
300.6°C at 760 mmHg  
Form:
Solid  
MP:
116.5 - 118 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
136  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
1.1  

Upstream Synthesis Route

[1]OrganicPreparationsandProceduresInternational,1999,vol.31,#1,p.120-123

[2]OrganicPreparationsandProceduresInternational,1999,vol.31,#1,p.120-123

[1]Patent:CN108586334,2018,A,.Locationinpatent:Paragraph0048-0050

[1]Tetrahedron,2013,vol.69,#33,p.6799-6803

[2]Patent:US5219847,1993,A,

[3]JournaloftheAmericanChemicalSociety,1952,vol.74,p.5967,5969

[4]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1984,#7,p.1501-1505

[5]BioorganicandMedicinalChemistry,2012,vol.20,#1,p.498-509

[1]Patent:EP1180514,2002,A1,.Locationinpatent:Example103

[2]YakugakuZasshi,1958,vol.78,p.661,665

[3]Chem.Abstr.,1958,p.18399

[1]RSCAdvances,2014,vol.4,#90,p.49395-49399

Downstream Synthesis Route

[1]Patent:EP1180514,2002,A1.Locationinpatent:Example103

[2]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1958,vol.78,p.661,665    Chem.Abstr.,1958,p.18399

[1]JournalofMedicinalChemistry,1984,vol.27,p.125-128

[2]Patent:US4404214,1983,A

[1]Patent:WO2018/17435,2018,A1.Locationinpatent:Paragraph00133-00134

[2]Patent:WO2015/94912,2015,A1.Locationinpatent:Page/Pagecolumn30-31

[3]Patent:EP1180514,2002,A1.Locationinpatent:Example103

[4]JournaloftheChemicalSociety.PerkintransactionsI,1984,p.1501-1505

[5]JournaloftheAmericanChemicalSociety,2017,vol.139,p.7745-7748

[6]Patent:WO2017/214359,2017,A1.Locationinpatent:Page/Pagecolumn83

[7]Patent:WO2012/106472,2012,A1.Locationinpatent:Page/Pagecolumn124

4021-07-2    543-27-1   
C12H15NO3 

[1]JournalofMedicinalChemistry,1984,vol.27,p.216-223

[1]OrganicPreparationsandProceduresInternational,1999,vol.31,p.120-123

[2]OrganicPreparationsandProceduresInternational,1999,vol.31,p.120-123

Literature

Title: Poly[[diaqua-tris-(μ(2)-3-methyl-pyridine-2-carboxyl-ato)(3-methyl-pyridine-2-car-boxyl-ato)sodiumterbium(III)] ethanol monosolvate monohydrate].

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: catena-Poly[sodium [[tris(3-methyl-pyridine-2-carboxylato)europate(III)]-μ-3-methylpyridine-2-carboxylato] trihydrate].

Journal: Acta crystallographica. Section E, Structure reports online 20100901

Title: Crystal structure, DNA binding studies, nucleolytic property and topoisomerase I inhibition of zinc complex with 1,10-phenanthroline and 3-methyl-picolinic acid.

Journal: Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine 20100201

Title: Design of a hairpin polyamide, ZT65B, for targeting the inverted CCAAT box (ICB) site in the multidrug resistant (MDR1) gene.

Journal: Chembiochem : a European journal of chemical biology 20051201

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SDS
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