CAS 31964-89-3

Phenol, 2-(2-amino-4-pyrimidinyl)-

Description:

Phenol, 2-(2-amino-4-pyrimidinyl)-, also known by its CAS number 31964-89-3, is an organic compound that features a phenolic structure substituted with a pyrimidine ring. This compound exhibits both acidic and basic properties due to the presence of the hydroxyl group (-OH) and the amino group (-NH2) on the pyrimidine ring. It is typically a solid at room temperature and is soluble in polar solvents, reflecting its ability to engage in hydrogen bonding. The presence of the amino group allows for potential interactions with biological systems, making it of interest in medicinal chemistry. Its structure suggests that it may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the reactivity of both the phenolic and pyrimidine components. Additionally, this compound may exhibit biological activity, which could be explored for pharmaceutical applications, particularly in the development of antimicrobial or anticancer agents. Safety data should be consulted for handling and usage, as with any chemical substance.

Formula: C₁₀H₉N₃O

2-(2-aminopyrimidin-4-yl)phenol

CAS: 31964-89-3

Formula: C₁₀H₉N₃O

Purity: 98%

Color and Shape: Solid

Molecular weight: 187.1980

Ref: IN-DA01C5MC

2-(2-Aminopyrimidin-4-yl)phenol

CAS: 31964-89-3

2-(2-Aminopyrimidin-4-yl)phenol

Purity: 97%

Molecular weight: 187.20g/mol

Ref: 54-OR13885

2-(2-aminopyrimidin-4-yl)phenol

CAS: 31964-89-3

2-(2-Aminopyrimidin-4-yl)phenol is an inhibitor of enzymes that catalyze the synthesis of nucleic acids. It inhibits the activity of DNA polymerase, RNA polymerase and ribonucleotide reductase. 2-(2-Aminopyrimidin-4-yl)phenol inhibits cell growth by blocking the production of nucleic acids, which are necessary for cellular division. This compound has potent inhibitory activity against tumor cells and may be useful as an antitumor agent.

Formula: C₁₀H₉N₃O

Purity: Min. 95%

Molecular weight: 187.19 g/mol

Ref: 3D-GBA96489