4-Pyrimidinamine, 2-fluoro- (9CI), with the CAS number 96548-91-3, is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. The presence of an amino group (-NH2) at the 4-position and a fluorine atom at the 2-position contributes to its reactivity and potential applications in pharmaceuticals and agrochemicals. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. Its fluorine substitution can influence its biological activity and lipophilicity, making it a subject of interest in medicinal chemistry. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

4-Pyrimidinamine, 2-fluoro- (9CI)

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2-Fluoropyrimidin-4-amine is a nucleoside analog that has been isolated from the hydrolysis of 2,6-difluoro-3,5-pyrimidinediamine. This compound has been shown to be an enolic hydroxy analog of cytosine and uracil. It is not known whether 2-fluoropyrimidin-4-amine can be converted into thymine.

CAS 96548-91-3: 4-Pyrimidinamine, 2-fluoro- (9CI)

2-Fluoropyrimidin-4-amine

Ref: 3D-WDA54891

2-Fluoropyrimidin-4-amine

Ref: IN-DA006QOP

2-FLUOROPYRIMIDIN-4-AMINE

Ref: 10-F473986

2-Fluoropyrimidin-4-amine

Ref: 54-PC408561