CAS 69879-22-7
:6-aminopyridine-3-carbaldehyde
Description:
6-Aminopyridine-3-carbaldehyde, with the CAS number 69879-22-7, is an organic compound characterized by its pyridine ring structure, which is substituted with an amino group and an aldehyde functional group. This compound typically appears as a solid or crystalline substance and is known for its potential applications in organic synthesis and medicinal chemistry. The presence of the amino group contributes to its basicity and reactivity, while the aldehyde group allows for various chemical transformations, such as condensation reactions. 6-Aminopyridine-3-carbaldehyde can participate in nucleophilic addition reactions and is often used as an intermediate in the synthesis of more complex molecules, including pharmaceuticals. Its solubility in polar solvents, such as water and alcohols, makes it versatile for various laboratory applications. Additionally, the compound's structure may influence its biological activity, making it a subject of interest in drug discovery and development. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C6H6N2O
InChI:InChI=1/C6H6N2O/c7-6-2-1-5(4-9)3-8-6/h1-4H,(H2,7,8)
InChI key:BMNPVMQSUPTGFD-UHFFFAOYSA-N
SMILES:c1cc(=N)[nH]cc1C=O
Synonyms:- 3-Pyridinecarboxaldehyde, 6-Amino-
- 6-Aminonicotinaldehyde
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Ref: IN-DA0065S2
250mg24.00€1g37.00€5g101.00€10g150.00€25g299.00€50g597.00€100g753.00€250g935.00€500g1,869.00€1kg3,433.00€6-Aminopyridine-3-carboxaldehyde
CAS:Controlled ProductApplications 6-Aminopyridine-3-carboxaldehyde is a novel ribonucleotide reductase inhibitor that belongs to the class of metal-binding site affecting ribonucleotide inhibitors that are derivatives of alpa-heterocyclic carboxaldehyde thiosemicarbazone.
References Lynn, F., et al.: Cancer. Chemother. Pharmacol., 50, 223 (2002);Formula:C6H6N2OColor and Shape:NeatMolecular weight:122.125





