Welcome to LookChem.com Sign In|Join Free
  • or
N-(Pyridin-4-yl)pyridine-4-carboxamide is a chemical compound with the formula C12H9N3O, characterized by its white to off-white powder form and a molecular weight of 211.22 g/mol. It is recognized for its potential biological activities, making it a significant compound in the realms of organic synthesis and pharmaceutical research.

64479-78-3

Post Buying Request

64479-78-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

64479-78-3 Usage

Uses

Used in Pharmaceutical Research:
N-(Pyridin-4-yl)pyridine-4-carboxamide is utilized as a research compound for its anti-cancer and anti-inflammatory properties, serving as a promising candidate for the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, N-(Pyridin-4-yl)pyridine-4-carboxamide is employed as a key intermediate, contributing to the creation of various complex organic molecules.
Used in Cancer Treatment:
N-(Pyridin-4-yl)pyridine-4-carboxamide is studied for its potential as an anti-cancer agent, targeting protein kinases that play a role in cellular processes often implicated in cancer.
Used in Inflammation Management:
N-(Pyridin-4-yl)pyridine-4-carboxamide is also considered for its anti-inflammatory applications, which could be beneficial in the treatment of various inflammatory conditions.
Overall, N-(Pyridin-4-yl)pyridine-4-carboxamide is a versatile chemical with significant potential across multiple industries, particularly in pharmaceuticals for the advancement of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 64479-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,7 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64479-78:
(7*6)+(6*4)+(5*4)+(4*7)+(3*9)+(2*7)+(1*8)=163
163 % 10 = 3
So 64479-78-3 is a valid CAS Registry Number.

64479-78-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-pyridin-4-ylpyridine-4-carboxamide

1.2 Other means of identification

Product number -
Other names 4-pyridylisonicotiamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64479-78-3 SDS

64479-78-3Relevant academic research and scientific papers

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)

Valverde-Mu?oz, Francisco Javier,Bartual-Murgui, Carlos,Pi?eiro-López, Lucía,Mu?oz, M. Carmen,Real, José Antonio

, p. 10038 - 10046 (2019)

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.

Synthesis and characterization of one, two and three-dimensional Cu(I) polymers supported by bipyridylamide ligands

Mugenzi, Clement,Powell, Douglas R.,Gerasimchuk, Nikolay N.,Yang, Lei

, p. 39 - 46 (2018/08/09)

Reaction of bipyridylamide ligands N-(3-pyridyl)nicotinamide (3-pna), N-(4-pyridyl)nicotinamide (4-pna) and N-(4-pyridyl)isonicotinamide (4-pina) with Cu(I) salts afforded four coordination polymers. X-ray crystallography analysis showed one-, two- and three-dimensional networks. The correlation between the pyridyl nitrogen donor disposition and dimensionality of the structures was discussed. Reflectance UV–Vis and fluorescence spectroscopic methods were used to characterize the MLCT features of these complexes. Thermal stability of the coordination polymers under nitrogen was also investigated.

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

Liu, Guofeng,Liu, Jinying,Feng, Chuanliang,Zhao, Yanli

, p. 1769 - 1775 (2017/03/09)

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,

INHIBITORS OF RHO ASSOCIATED PROTEIN KINASES (ROCK) AND METHODS OF USE

-

Page/Page column 42, (2013/08/15)

Compounds and compositions having activity as inhibitors of Rho-associated proteinkinases (ROCKs), and methods of making and using the subject compounds are disclosed.

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

Nebot, Vicent J.,Armengol, Jose,Smets, Johan,Prieto, Susana Fernandez,Escuder, Beatriu,Miravet, Juan F.

supporting information; experimental part, p. 4063 - 4072 (2012/05/31)

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

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 64479-78-3