CAS 116941-10-7
:Cyclohexanecarboxamide, 4-hydroxy-, trans- (9CI)
Description:
Cyclohexanecarboxamide, 4-hydroxy-, trans- (9CI) is an organic compound characterized by its cyclohexane ring structure with a carboxamide functional group and a hydroxyl group positioned at the fourth carbon in a trans configuration. This compound is typically a white to off-white solid and is soluble in polar solvents due to the presence of the hydroxyl and amide groups, which can engage in hydrogen bonding. Its molecular structure contributes to its potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the hydroxyl group enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. Additionally, the trans configuration is significant as it can affect the compound's physical properties and interactions with biological targets. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards. Overall, Cyclohexanecarboxamide, 4-hydroxy-, trans- is a compound of interest due to its unique structural features and potential applications.
Formula:C7H13NO2
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Found 1 products.
4-Hydroxycyclohexane-1-carboxamide
CAS:4-Hydroxycyclohexane-1-carboxamide is a derivative of cyclohexane. It is a potent inhibitor of the enzyme monoamine oxidase (MAO) and has been used in positron emission studies to study MAO activity in rat hepatocytes. The compound has also been shown to inhibit the linkage of 5HT1A receptors with phospholipase C, which may be due to its ability to inhibit amine uptake. 4-Hydroxycyclohexane-1-carboxamide metabolizes rapidly in humans, but not in rats. Studies have shown that it hydrolyzes quickly into an amide form when exposed to human erythrocytes, whereas it does not react with rat erythrocytes.Formula:C7H13NO2Purity:Min. 95%Molecular weight:143.19 g/mol
