CAS 82261-42-5

4-(pyridin-3-yl)aniline

Description:

4-(Pyridin-3-yl)aniline, with the CAS number 82261-42-5, is an organic compound characterized by the presence of both an aniline and a pyridine functional group. This compound features a pyridine ring substituted at the 3-position with an aniline group, which consists of a phenyl ring attached to an amino group. The molecular structure contributes to its potential applications in various fields, including pharmaceuticals and materials science. It typically exhibits properties such as moderate solubility in organic solvents and may participate in hydrogen bonding due to the amino group. The presence of the pyridine ring can influence its electronic properties, making it a candidate for coordination with metal ions or as a ligand in coordination chemistry. Additionally, the compound may display biological activity, which can be explored in medicinal chemistry. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₁H₁₀N₂

InChI: InChI=1/C11H10N2/c12-11-5-3-9(4-6-11)10-2-1-7-13-8-10/h1-8H,12H2

SMILES: c1cc(cnc1)c1ccc(cc1)N

Synonyms:

• 3-(p-Aminophenyl)pyridine
• Benzenamine, 4-(3-pyridinyl)-
• 3-(4-Aminophenyl)pyridine
• 4-(3-Pyridyl)Aniline
• 4-Pyridin-3-ylaniline
• 4-(Pyridin-3-yl)aniline

4-Pyridin-3-ylaniline

CAS: 82261-42-5

Formula: C₁₁H₁₀N₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 170.2105

Ref: IN-DA0055ZI

4-(Pyridin-3-yl)aniline

CAS: 82261-42-5

4-(Pyridin-3-yl)aniline

Formula: C₁₁H₁₀N₂

Purity: ≥95%

Color and Shape: yellow crystalline powder

Molecular weight: 170.21g/mol

Ref: 54-OR2020

4-(3-Pyridyl)aniline

CAS: 82261-42-5

4-(3-Pyridyl)aniline is a chemical compound that belongs to the group of inhibitors. It is structurally related to the pyridine and aniline rings. 4-(3-Pyridyl)aniline has been shown to inhibit protein kinases, such as casein kinase II and glycogen synthase kinase 3β, in the presence of ATP. The crystallography studies have shown that 4-(3-pyridyl)aniline binds tightly to the ATP binding site of these enzymes by occupying the same position as ATP and forming hydrogen bonds with residues at this site. Structural analysis has also demonstrated that 4-(3-pyridyl)aniline binds to other sites on these enzymes, including the ATP phosphate binding site, which may account for its inhibitory activity against both type 1 and type 2 protein kinases.

Formula: C₁₁H₁₀N₂

Purity: Min. 95%

Molecular weight: 170.22 g/mol

Ref: 3D-HDA26142

4-Pyridin-3-ylphenylamine

CAS: 82261-42-5

Formula: C₁₁H₁₀N₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 170.215

Ref: 10-F034277