《Studies on synthesis and anticancer activity of selected N-(2-fluoroethyl)-N-nitrosoureas》 was published in Journal of Medicinal Chemistry in 1984. These research results belong to Johnston, Thomas P.; Kussner, Conrad L.; Carter, Ronald L.; Frye, Jerry L.; Lomax, Nancita R.; Plowman, Jacqueline; Narayanan, V. L.. Recommanded Product: Benzyl (2,6-dioxopiperidin-3-yl)carbamate The article mentions the following:
Aminolysis of FCH2CH2N(NO)CO2C6H4NO2-2 with H2NCH2CH2OH, 1α,2β,3α-2-amino-1,3-cyclohexanediol, cis-1,2-aminocyclohexanol, and 2-amino-2-deoxy-D-glucose gave the corresponding H2O-sol ureas, e.g., I. The H2O-insoluble glutarimide analog II was prepared by nitrosation of the corresponding urea. In trials with B16 melanoma and Lewis lung carcinoma the compounds were comparable to their Cl analogs as inhibitors; I seemed to be the most effective. In the experimental materials used by the author, we found Benzyl (2,6-dioxopiperidin-3-yl)carbamate(cas: 24666-55-5Recommanded Product: Benzyl (2,6-dioxopiperidin-3-yl)carbamate)
Benzyl (2,6-dioxopiperidin-3-yl)carbamate(cas: 24666-55-5) belongs to anime. In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair. Amines are formally derivatives of ammonia (NH3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group (these may respectively be called alkylamines and arylamines; amines in which both types of substituent are attached to one nitrogen atom may be called alkylarylamines).Recommanded Product: Benzyl (2,6-dioxopiperidin-3-yl)carbamate
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem