2-(4,6-Dimethylpyrimidin-2-yl)-1-phenylguanidine, with the CAS number 16018-49-8, is a chemical compound characterized by its unique structure that includes a pyrimidine ring and a guanidine moiety. This compound typically exhibits properties such as being a solid at room temperature, with potential applications in medicinal chemistry due to its biological activity. The presence of the dimethyl groups on the pyrimidine ring can influence its solubility and reactivity, while the phenyl group contributes to its hydrophobic characteristics. It may also engage in hydrogen bonding due to the guanidine functional group, which can enhance its interactions with biological targets. Additionally, this compound may exhibit specific pharmacological properties, making it of interest in drug development. Its synthesis and characterization would involve standard organic chemistry techniques, and it may be analyzed using methods such as NMR spectroscopy, mass spectrometry, and chromatography to confirm its purity and structural integrity. Overall, this compound represents a class of organic molecules that can be explored for various chemical and biological applications.

2-(4,6-dimethylpyrimidin-2-yl)-1-phenylguanidine

16018-49-8: 1-(4,6-Dimethylpyrimidin-2-yl)-3-phenylguanidine, Guanidine, N-(4,6-dimethyl-2-pyrimidinyl)-N'-phenyl-, N-(4,6-Dimethyl-pyrimidin-2-yl)-N'-phenyl-guanidine

Guanidine, N-(4,6-dimethyl-2-pyrimidinyl)-N'-phenyl-

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CAS 16018-49-8: 2-(4,6-dimethylpyrimidin-2-yl)-1-phenylguanidine

Guanidine, N-(4,6-dimethyl-2-pyrimidinyl)-N'-phenyl-

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N-(4,6-Dimethylpyrimidin-2-yl)-N'-phenylguanidine

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