256005
2,6-Pyridinedicarboxaldehyde
97%
Synonym(s):
2,6-Bis(formyl)pyridine, 2,6-Diformylpyridine, 2,6-Pyridinedialdehyde, Pyridine-2,6-dicarbaldehyde
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About This Item
Recommended Products
Quality Level
Assay
97%
form
solid
bp
152-154 °C/103 mmHg (lit.)
mp
124-125 °C (lit.)
functional group
aldehyde
storage temp.
2-8°C
SMILES string
[H]C(=O)c1cccc(n1)C([H])=O
InChI
1S/C7H5NO2/c9-4-6-2-1-3-7(5-10)8-6/h1-5H
InChI key
PMWXGSWIOOVHEQ-UHFFFAOYSA-N
General description
2,6-Pyridinedicarboxaldehyde can serve as a building block in the synthesis of various organic compounds.
Application
2,6-Pyridinedicarboxaldehyde has been used in preparation of:
- functionalized resin Amberlite XAD-4
- boron-dipyrromethene (BODIPY)-based fluorescence probe with a N,N′-(pyridine-2, 6-diylbis(methylene))-dianiline substituent
- novel N-heterocyclic chitosan aerogel derivatives
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Food chemistry, 141(2), 655-661 (2013-06-26)
The synthesis and characterization of the resin Amberlite XAD-4 functionalized with 2,6-pyridinedicarboxaldehyde and its application in an on-line system for the preconcentration of cadmium, cobalt, copper, lead and manganese prior to determination using flame atomic absorption spectrometry (FAAS) is proposed.
Journal of fluorescence, 26(1), 11-22 (2015-11-21)
Herein, we reported the ditriazole Schiff base derivative 1 and evaluated its photophysical properties on induction of varieties of metal ions including Na(+), Ag(+), Ni(2+), Mn(2+), Pd(2+), Co(2+), Hg(2+), Cu(2+), Pb(2+), Cd(2+), Zn(2+), Sn(2+), Fe(2+), Fe(3+), Cr(3+) and Al(3+), in
International journal of biological macromolecules, 45(4), 330-337 (2009-08-12)
The novel N-heterocyclic chitosan aerogel derivatives were prepared by reacting 79% deacetylated chitosan separately with 4-pyridinecarboxaldehyde and 2,6-pyridinedicarboxaldehyde followed by subsequent solvent exchange into acetone, filteration and lyophilization. The identity of the Schiff bases was confirmed by UV-vis absorption spectroscopy
The journal of physical chemistry. A, 113(51), 14081-14086 (2009-12-03)
A boron-dipyrromethene (BODIPY)-based fluorescence probe with a N,N'-(pyridine-2, 6-diylbis(methylene))-dianiline substituent (1) has been prepared by condensation of 2,6-pyridinedicarboxaldehyde with 8-(4-amino)-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene and reduction by NaBH(4). The sensing properties of compound 1 toward various metal ions are investigated via fluorometric titration in
Molecules (Basel, Switzerland), 24(2) (2019-01-19)
The present study focuses on the design and synthesis of a cage-like organic skeleton containing two triazole rings jointed via imine linkage. These molecules can act as urease inhibitors. The in-vitro urease inhibition screening results showed that the combination of
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