2-(4-Morpholine)ethyl bromide, with the CAS number 89583-07-3, is an organic compound characterized by its structure, which includes a morpholine ring and a bromide substituent. This compound typically appears as a colorless to pale yellow liquid and is soluble in polar solvents due to the presence of the morpholine moiety, which enhances its polarity. The morpholine group contributes to its basicity and potential reactivity, making it a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The bromide atom serves as a good leaving group, facilitating nucleophilic substitution reactions. Additionally, 2-(4-Morpholine)ethyl bromide may exhibit moderate toxicity, necessitating careful handling and appropriate safety measures in laboratory settings. Its chemical properties, such as boiling point and density, can vary based on purity and environmental conditions. Overall, this compound is significant in synthetic organic chemistry and has applications in various fields, including medicinal chemistry and materials science.

2-(4-Morpholine)ethyl bromide

89583-07-3: 2-Morpholinoethyl Bromide, 4-(2-Bromoethyl)morpholine, Morpholine, 4-(2-Bromoethyl)-

4-(2-bromoethyl)morpholine

4-(2-Bromoethyl)morpholine

2-(4-Morpholine)ethylbromide

4-(2-Bromoethyl)morpholine is a potential anticancer agent that has been found to inhibit the viability of human cancer cells in vitro. It is believed to be an anticancer drug because it binds to the CB2 receptor and inhibits the production of collagen, which is needed for tumor growth. 4-(2-Bromoethyl)morpholine has been shown to inhibit platelet aggregation and reduce blood viscosity, making it a possible treatment for coronary heart disease. It also inhibits the release of nitric oxide, which can lead to atherosclerosis. 4-(2-Bromoethyl)morpholine has been synthesized by reacting methylamine with morpholine in the presence of nitrogen gas at high temperature and pressure. This reaction produces a gaseous product that is then condensed into nanocarriers that are soluble in water. The acidic nature of this compound may introduce imidazole derivatives as prodrugs for its activity.

CAS 89583-07-3: 2-(4-Morpholine)ethyl bromide

4-(2-bromoethyl)morpholine

Ref: IN-DA00369N

4-(2-Bromoethyl)morpholine

Ref: 54-OR92647

2-(4-Morpholine)ethylbromide

Ref: 10-F078086

4-(2-Bromoethyl)morpholine

Ref: 3D-FB139679