2-Amino-3-Pyridinecarboxaldehyde CAS#7521-41-7
2-Amino-3-Pyridinecarboxaldehyde CAS#7521-41-7 Promotion Season Now in Store and Free Sample for Testing with Factory Price
Chemical Name:2-Amino-3-Pyridinecarboxaldehyde
CAS No.:7521-41-7
Molecular Formula:C6H6N2O
Molecular weight:122.12
Sample:Available
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Products Description of 2-Amino-3-Pyridinecarboxaldehyde CAS#7521-41-7
2-Amino-3-pyridinecarboxaldehyde is a pyridine derivative with significant alkalinity, commonly used in organic synthesis and pharmaceutical chemical intermediates. It can synthesize organic compounds with pyridine skeletons through various chemical reactions such as condensation reaction, cyclization reaction and substitution reaction. It has a wide range of applications in basic chemical research. 2-Amino-3-pyridinecarboxaldehyde has rich chemical transformation properties, which contains pyridine units, amino groups and highly chemically reactive aldehyde groups. It should be noted that this substance is sensitive to oxidants and is easily oxidized to nitrogen oxides by oxidants and deteriorates.
2-Amino-3-Pyridinecarboxaldehyde CAS#7521-41-7 Chemical Properties
Melting point | 98-102 °C (lit.) |
Boiling point | 290.7±25.0 °C(Predicted) |
density | 1.264±0.06 g/cm3(Predicted) |
Fp | >300℃ |
storage temp. | Keep in dark place,Sealed in dry,Room Temperature |
solubility | Chloroform (Slightly), Methanol (Slightly) |
pka | 4.99±0.36(Predicted) |
form | Powder, Crystals and/or Chunks |
color | Yellow to light brown |
Water Solubility | insoluble |
Sensitive | Air Sensitive |
BRN | 109598 |
InChIKey | NXMFJCRMSDRXLD-UHFFFAOYSA-N |
CAS DataBase Reference | 7521-41-7(CAS DataBase Reference) |
Safety Information
Hazard Codes | Xi,Xn |
Risk Statements | 36/37/38-20/21/22 |
Safety Statements | 26-36-36/37/39 |
WGK Germany | 3 |
HazardClass | IRRITANT |
PackingGroup | II |
HS Code | 29339900 |
Product Application of 2-Amino-3-Pyridinecarboxaldehyde CAS#7521-41-7
2-Amino-3-pyridinecarboxaldehyde can be used to synthesize pyridine organic ligands and functional organic small molecules through chemical conversion reactions of amino groups and aldehyde groups. These organic ligands have a wide range of applications in coordination chemistry and coordination catalysis, and can be used for the coordination and catalytic reactions of metal ions, thereby achieving high selectivity and high efficiency in organic synthesis. Through chemical conversion reactions, different functional groups can be introduced into the pyridine ring in the structure of the compound, thereby constructing various functional organic small molecules, which have potential applications in the fields of materials science, optoelectronic devices, sensors and biology, such as fluorescent probes, bioactive molecules and functional materials.
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