2-Amino-3-Pyridinecarboxaldehyde

1.Multi-Functional Pharmaceutical Building Block: Extensively applied in organic synthesis and acts as a crucial intermediate for pharmaceutical molecules.

2.Diverse Chemical Reactivity: Possesses pyridine, amino and aldehyde functional groups, allowing a wide range of reactions including condensation, cyclization and substitution.

3.High Suitability for Research Purposes: Its flexible structural conversion properties make it ideal for fundamental chemical research.

4.Key Precursor for Pyridine-Based Derivatives: Enables the preparation of numerous pyridine-structured compounds, advancing high-level chemical development.

Product Description

2-Amino-3-pyridinecarboxaldehyde is an alkaline pyridine-based derivative that is extensively employed in organic synthesis and serves as a key pharmaceutical intermediate. It can form pyridine-containing organic molecules via condensation, cyclization, substitution and other reactions, rendering it highly valuable for fundamental chemical research. Its molecular structure contains several reactive functional groups, namely a pyridine ring, an amino group and a highly reactive aldehyde group, which support a broad range of chemical conversions. Notably, this compound is susceptible to oxidizing agents and may degrade upon easy oxidation into nitrogen oxides.

2-Amino-3-Pyridinecarboxaldehyde

 Product Parameter

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)
pka4.99±0.36(Predicted)
form Powder, Crystals and/or Chunks
color Yellow to light brown
Water Solubility insoluble
Sensitive Air Sensitive
BRN 109598
InChIKeyNXMFJCRMSDRXLD-UHFFFAOYSA-N
CAS DataBase Reference7521-41-7(CAS DataBase Reference)
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

Chemical Properties

2-Amino-3-pyridinecarboxaldehyde can be employed to prepare pyridine-type organic ligands and functional small molecules by utilizing its amino and aldehyde functional groups. Such ligands are extensively used in coordination chemistry and catalysis, capable of coordinating effectively with metal ions to drive highly selective and efficient catalytic reactions in organic synthesis.

Moreover, diverse functional groups can be grafted onto the pyridine ring through chemical modification, facilitating the construction of a wide range of functionalized molecules. These compounds hold promising applications in materials science, optoelectronic devices, sensors and biological fields, such as fluorescent probes, bioactive agents and high-performance functional materials.

2-Amino-3-Pyridinecarboxaldehyde

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