1-(2-Fluoroethyl)-1-nitroso-3-[4-(propan-2-yl)cyclohexyl]urea, with the CAS number 33024-38-3, is a synthetic organic compound characterized by its unique molecular structure, which includes a nitroso group and a urea moiety. This compound features a fluoroethyl substituent, which can influence its reactivity and biological activity. The presence of the cyclohexyl group, substituted with an isopropyl group, contributes to its steric properties and may affect its interaction with biological targets. Generally, compounds of this nature may exhibit potential pharmacological activities, including antitumor or antimicrobial properties, although specific biological data for this compound may be limited. Its chemical stability, solubility, and reactivity can vary based on environmental conditions and the presence of other functional groups. As with many synthetic urea derivatives, it is essential to handle this compound with care, considering potential toxicity and environmental impact. Further research would be necessary to fully elucidate its properties and potential applications in medicinal chemistry or other fields.

1-(2-fluoroethyl)-1-nitroso-3-[4-(propan-2-yl)cyclohexyl]urea

33024-38-3: 1-(2-Fluoroethyl)-3-(4-isopropylcyclohexyl)-1-nitrosourea, urea, N-(2-fluoroethyl)-N'-[4-(1-methylethyl)cyclohexyl]-N-nitroso-

The compound 1-(2-fluoroethyl)-1-nitroso-3-(4-propan-2-ylcyclohexyl)urea is a quinolizidine alkaloid. The conformational and stereochemical properties of the molecule are determined by the stereoisomers, which are a result of the isomerization of the sulfate group. The molecule has a dipole moment due to its molecular structure, which allows it to be used as a catalyst for organic reactions. This compound also absorbs light at wavelengths of 260 nm and 285 nm. The thermal isomerization reaction can be catalyzed by copper chromite.

CAS 33024-38-3: 1-(2-fluoroethyl)-1-nitroso-3-[4-(propan-2-yl)cyclohexyl]urea

1-(2-Fluoroethyl)-1-Nitroso-3-(4-Propan-2-Ylcyclohexyl)Urea

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