CAS 78473-10-6

2-amino-3,5-dicyanopyridinium

Description:

2-Amino-3,5-dicyanopyridinium, identified by its CAS number 78473-10-6, is a chemical compound that features a pyridine ring substituted with two cyano groups and an amino group. This compound is characterized by its strong electron-withdrawing cyano groups, which significantly influence its reactivity and stability. The presence of the amino group provides basic properties, allowing it to participate in various chemical reactions, including nucleophilic substitutions. The dicyanopyridinium structure contributes to its potential applications in organic synthesis, particularly in the development of dyes, pharmaceuticals, and agrochemicals. Additionally, the compound may exhibit interesting electronic properties due to the conjugation within the aromatic system, making it a subject of interest in materials science and coordination chemistry. Its solubility and stability in different solvents can vary, which is essential for its practical applications. Overall, 2-amino-3,5-dicyanopyridinium is a versatile compound with significant potential in various chemical fields.

Formula: C₇H₅N₄

InChI: InChI=1/C7H4N4/c8-2-5-1-6(3-9)7(10)11-4-5/h1,4H,(H2,10,11)/p+1

2-Aminopyridine-3,5-dicarbonitrile

CAS: 78473-10-6

Formula: C₇H₄N₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 144.1335

Ref: IN-DA00539J

2-Aminopyridine-3,5-dicarbonitrile

CAS: 78473-10-6

2-Aminopyridine-3,5-dicarbonitrile

Purity: 97%

Molecular weight: 144.14g/mol

Ref: 54-OR1054441

2-aminopyridine-3,5-dicarbonitrile

CAS: 78473-10-6

Formula: C₇H₄N₄

Purity: ≥97%

Color and Shape: Solid

Molecular weight: 144.137

Ref: 10-F521222

2-Amino-3,5-pyridinedicarbonitrile

Controlled Product

CAS: 78473-10-6

Formula: C₇H₄N₄

Color and Shape: Neat

Molecular weight: 144.133

Ref: TR-A191841

2-Amino-3,5-pyridinedicarbonitrile

CAS: 78473-10-6

2-Amino-3,5-pyridinedicarbonitrile (APDC) is a small molecule that has been shown to bind to the adenosine A1 receptor with high affinity and selectivity. It has a molecular weight of 167.2 g/mol, a pK of 7.4 and a logP value of 2.8. APDC was first synthesized in 1963 by scientists at the National Institute for Medical Research in London. The chlorine atom is influential in the pharmacokinetics of this compound. The pharmacokinetic profile shows that APDC is poorly absorbed and eliminated quickly from the body, with an elimination half-life of 0.6 hours and an oral bioavailability of less than 1%. This drug also has multipotent effects on Alzheimer's disease, showing significant efficacy against both plaques and tangles in animal models of Alzheimer's disease.

Formula: C₇H₄N₄

Purity: Min. 95%

Molecular weight: 144.13 g/mol

Ref: 3D-DDA47310