2-Pyrimidinamine, 4-chloro-N,N-dimethyl- is an organic compound characterized by its pyrimidine ring structure, which is a six-membered heterocyclic aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a chloro substituent at the 4-position and dimethylamino groups at the 2-position contributes to its chemical reactivity and potential applications. 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. It can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it of interest in medicinal chemistry and the development of pharmaceuticals. The compound's structure suggests potential biological activity, which may be explored in drug discovery contexts. Safety data should be consulted for handling and usage, as halogenated compounds can pose environmental and health risks. Overall, 2-Pyrimidinamine, 4-chloro-N,N-dimethyl- is a notable compound in the realm of organic synthesis and medicinal chemistry.

2-Pyrimidinamine, 4-chloro-N,N-dimethyl-

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(4-Chloro-pyrimidin-2-yl)-dimethyl-amine

(4-Chloro-pyrimidin-2-yl)-dimethyl-amine is a versatile compound with a wide range of applications. It acts as a solid catalyst in various chemical reactions and is commonly used in organometallic chemistry. This compound is also classified as a research chemical and is often utilized in the development of new catalysts and materials.

In addition to its role as a catalyst, (4-Chloro-pyrimidin-2-yl)-dimethyl-amine has shown potential therapeutic properties. It interacts with dopamine receptors, which are involved in various neurological processes. This compound has been studied for its potential use as a medicament or treatment for certain neurological disorders.

Furthermore, (4-Chloro-pyrimidin-2-yl)-dimethyl-amine has demonstrated excellent transport properties, making it suitable for applications in the field of glycan research. Its ability to enhance the transport of glycan molecules across cell membranes has significant implications for the

CAS 23631-02-9: 2-Pyrimidinamine, 4-chloro-N,N-dimethyl-

(4-Chloro-pyrimidin-2-yl)-dimethyl-amine

Ref: 10-F085108

(4-Chloro-pyrimidin-2-yl)-dimethyl-amine

Ref: 3D-YAA63102

2-Pyrimidinamine, 4-chloro-N,N-dimethyl-

Ref: IN-DA002NY6

4-Chloro-N,N-dimethylpyrimidin-2-amine

Ref: 54-OR93358