CAS 57356-49-7
:N-Phenyl-2-pyrimidinamine
Description:
N-Phenyl-2-pyrimidinamine, with the CAS number 57356-49-7, is an organic compound characterized by its pyrimidine ring structure substituted with a phenyl group and an amino group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential solubility in organic solvents and moderate stability under standard conditions. It may participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions, due to the presence of the amino group. The compound's structure suggests potential applications in pharmaceuticals or agrochemicals, as derivatives of pyrimidine and aniline are often explored for their biological activities. Additionally, N-Phenyl-2-pyrimidinamine may exhibit specific spectral characteristics in techniques such as NMR and IR spectroscopy, aiding in its identification and characterization. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C10H9N3
InChI:InChI=1S/C10H9N3/c1-2-5-9(6-3-1)13-10-11-7-4-8-12-10/h1-8H,(H,11,12,13)
InChI key:InChIKey=XGXNTJHZPBRBHJ-UHFFFAOYSA-N
SMILES:N(C1=CC=CC=C1)C=2N=CC=CN2
Synonyms:- 2-(Phenylamino)pyrimidine
- 2-Anilinopyrimidine
- 2-Pyrimidinamine, N-phenyl-
- N-Phenylpyrimidin-2-amine
- Pyrimidine, 2-anilino-
- N-Phenyl-2-pyrimidinamine
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Found 4 products.
N-Phenyl-2-Pyrimidinamine
CAS:Formula:C10H9N3Purity:98%Color and Shape:SolidMolecular weight:171.1986N-Phenylpyrimidin-2-amine
CAS:Controlled Product<p>Applications N-Phenylpyrimidin-2-amine is used in preparation of Nitrogen-containing Heterocyclic Hexafluoroborate.<br>References Cui, Y., et al.: Faming Zhuanli Shenqing, (2019);<br></p>Formula:C10H9N3Color and Shape:NeatMolecular weight:171.199
