CAS 22961-45-1
:N-Phenyl-4-pyridinamine
Description:
N-Phenyl-4-pyridinamine, also known by its CAS number 22961-45-1, is an organic compound characterized by the presence of both a phenyl group and a pyridinamine moiety. This compound features a pyridine ring substituted with an amino group at the 4-position and a phenyl group at the nitrogen atom. It typically appears as a solid or crystalline substance and is soluble in organic solvents. The presence of the amino group contributes to its basicity and potential reactivity, making it a candidate for various chemical reactions, including those involving electrophilic aromatic substitution. N-Phenyl-4-pyridinamine may exhibit biological activity, which can be of interest in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its structural characteristics allow for potential interactions with biological molecules, making it a subject of study 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=1S/C11H10N2/c1-2-4-10(5-3-1)13-11-6-8-12-9-7-11/h1-9H,(H,12,13)
InChI key:InChIKey=DKQSRQLSDPYGCJ-UHFFFAOYSA-N
SMILES:N(C1=CC=CC=C1)C=2C=CN=CC2
Synonyms:- N-Phenyl-4-pyridinamine
- 4-(Phenylamino)pyridine
- Pyridine, 4-anilino-
- 4-Anilinopyridine
- 4-Pyridinamine, N-phenyl-
- N-phenylpyridin-4-amine
- phenyl-(4-pyridyl)amine
- N-(4-Pyridyl)aniline
- AKOS BC-0724
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Found 5 products.
4-Anilinopyridine
CAS:Formula:C11H10N2Purity:>98.0%(GC)(T)Color and Shape:White to Orange to Green powder to crystallineMolecular weight:170.224-Pyridinamine, N-phenyl-
CAS:Formula:C11H10N2Purity:95%Color and Shape:SolidMolecular weight:170.2105N-Phenylpyridin-4-amine
CAS:<p>N-Phenylpyridin-4-amine is a tautomeric compound that has been shown to inhibit the growth of cancer cells. It is able to bind to tyrosine kinase and inhibit its activity, which affects the proliferation of cancer cells. N-Phenylpyridin-4-amine also inhibits mitochondrial functions by inhibiting cytochrome c oxidase. This drug also has an anti-inflammatory effect, inhibiting the production of cytokines such as IL1β, IL6, and TNFα. The biological function of N-Phenylpyridin-4-amine is not yet fully understood. It may be due to the inhibition of protein tyrosine phosphatases (such as PTP1B), which are involved in insulin signalling pathways.</p>Formula:C11H10N2Purity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:170.21 g/mol




