Home Carboxys 2,4-Pyridinedicarboxylic acid

2,4-Pyridinedicarboxylic acid

CAS No.:
499-80-9
Catalog Number:
AG00I8WK
Molecular Formula:
C7H5NO4
Molecular Weight:
167.1189
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$13
- +
5g
95%
In Stock USA
United States
$38
- +
25g
95%
In Stock USA
United States
$125
- +
100g
95%
In Stock USA
United States
$363
- +
Product Description
Catalog Number:
AG00I8WK
Chemical Name:
2,4-Pyridinedicarboxylic acid
CAS Number:
499-80-9
Molecular Formula:
C7H5NO4
Molecular Weight:
167.1189
MDL Number:
MFCD00149413
IUPAC Name:
pyridine-2,4-dicarboxylic acid
InChI:
InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12)
InChI Key:
MJIVRKPEXXHNJT-UHFFFAOYSA-N
SMILES:
OC(=O)c1ccnc(c1)C(=O)O
EC Number:
207-892-2
UNII:
AFI29F0TVL
NSC Number:
403248
Properties
Complexity:
204  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
167.022g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
167.12g/mol
Monoisotopic Mass:
167.022g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
87.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  
Literature
Title Journal
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The synthesis, spectroscopic, X-ray characterization and in vitro cytotoxic testing results of activity of five new trans-platinum(IV) complexes with functionalized pyridines. European journal of medicinal chemistry 20120901
Studies of H3K4me3 demethylation by KDM5B/Jarid1B/PLU1 reveals strong substrate recognition in vitro and identifies 2,4-pyridine-dicarboxylic acid as an in vitro and in cell inhibitor. The FEBS journal 20120601
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Structural basis for binding of cyclic 2-oxoglutarate analogues to factor-inhibiting hypoxia-inducible factor. Bioorganic & medicinal chemistry letters 20101015
Characterization of two carnation petal prolyl 4 hydroxylases. Physiologia plantarum 20101001
A red zwitterionic co-crystal of acetaminophen and 2,4-pyridinedicarboxylic acid. Journal of pharmaceutical sciences 20100901
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Design, synthesis, enzyme-inhibitory activity, and effect on human cancer cells of a novel series of jumonji domain-containing protein 2 histone demethylase inhibitors. Journal of medicinal chemistry 20100812
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A cocrystal of pyridine-2,4-dicarboxylic acid and serine. Acta crystallographica. Section E, Structure reports online 20080101
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Properties