64479-78-3

Basic information

• Product Name: N-(Pyridin-4-yl)pyridine-4-carboxamide
• Synonyms: N-(Pyridin-4-yl)pyridine-4-carboxamide;4-Pyridinecarboxamide, N-4-pyridinyl-
• CAS NO: 64479-78-3
• Molecular Formula: C₁₁H₉N₃O
• Molecular Weight: 199.20866
• Mol File: 64479-78-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 196 °C
• Boiling Point: 286.1±15.0 °C(Predicted)
• Appearance: /
• Density: 1.287±0.06 g/cm3(Predicted)
• PKA: 10.94±0.70(Predicted)
• CAS DataBase Reference: N-(Pyridin-4-yl)pyridine-4-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Pyridin-4-yl)pyridine-4-carboxamide(64479-78-3)
• EPA Substance Registry System: N-(Pyridin-4-yl)pyridine-4-carboxamide(64479-78-3)

Safety Data

• Hazardous Substances Data: 64479-78-3(Hazardous Substances Data)

Usage

General Description

N-(Pyridin-4-yl)pyridine-4-carboxamide is a chemical compound with the formula C12H9N3O. It is a white to off-white powder with a molecular weight of 211.22 g/mol. N-(Pyridin-4-yl)pyridine-4-carboxamide is often used in organic synthesis and pharmaceutical research due to its potential biological activities. N-(Pyridin-4-yl)pyridine-4-carboxamide has been studied for its anti-cancer and anti-inflammatory properties, making it a promising candidate for drug development. Additionally, it has been investigated for its role as a potential inhibitor of protein kinases, which are involved in various cellular processes and are often targeted in cancer treatments. Overall, N-(Pyridin-4-yl)pyridine-4-carboxamide is an important chemical compound with potential applications in various fields, especially in the development of new pharmaceuticals.

Upstream product

• 504-24-5 4-aminopyridine 
• 39178-35-3 isonicotinoyl chloride hydrochloride 
• 55-22-1 pyridine-4-carboxylic acid 

Downstream Products

• 951224-76-3 Zn(tetraphenylporphyrinato)(N-(4-pyridyl)isonicotinamide)*(p-xylene)*(2-p-tolylethenol) 

Relevant articles and documents

Influence of Host-Guest and Host-Host Interactions on the Spin-Crossover 3D Hofmann-type Clathrates {FeII(pina)[MI(CN)2]2}· xMeOH (MI = Ag, Au)

The synthesis, structural characterization and magnetic properties of two new isostructural porous 3D compounds with the general formula {FeII(pina)[MI(CN)2]2}·xMeOH (x = 0-5; pina = N-(pyridin-4-yl)isonicotinamide; MI = AgI and x ～5 (1·xMeOH); MI = AuI and x ～5 (2·xMeOH)) are presented. The single-crystal X-ray diffraction analyses have revealed that the structure of 1·xMeOH (or 2·xMeOH) presents two equivalent doubly interpenetrated 3D frameworks stabilized by both argentophilic (or aurophilic) interactions and interligand C=O···HC H-bonds. Despite the interpenetration of the networks, these compounds display accessible void volume capable of hosting up to five molecules of methanol which interact with the host pina ligand and establish an infinite lattice of hydrogen bonds along the structural channels. Interestingly, the magnetic studies have shown that solvated complexes 1·xMeOH and 2·xMeOH display two- and four-step hysteretic thermally driven spin transitions, respectively. However, when these compounds lose the methanol molecules, the magnetic behavior changes drastically giving place to gradual spin conversions evidencing the relevant influence of the guest molecules on the spin-crossover properties. Importantly, since the solvent desorption takes place following a single-crystal-to-single-crystal transformation, empty structures 1 and 2 (x = 0) could be also determined allowing us to evaluate the correlation between the structural changes and the modification of the magnetic properties triggered by the loss of methanol molecules.

Unexpected right-handed helical nanostructures co-assembled from l-phenylalanine derivatives and achiral bipyridines

The construction of chiral supramolecular systems with desirable handedness is of great importance in materials science, chemistry, and biology since chiral nanostructures exhibit fascinating photophysical properties and unique biological effects. Herein,

Molecular hydrogels from bolaform amino acid derivatives: A structure-properties study based on the thermodynamics of gel solubilization

Insight is provided into the aggregation thermodynamics associated to hydrogel formation by molecular gelators derived from L-valine and L-isoleucine. Solubility data from NMR measurements are used to extract thermodynamic parameters for the aggregation i