
CAS 1289585-01-8
:(S)-3-(6-Chloro-pyrimidin-4-ylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester
Description:
(S)-3-(6-Chloro-pyrimidin-4-ylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester is a chemical compound characterized by its specific stereochemistry and functional groups. It features a pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle, and a tert-butyl ester group that enhances its lipophilicity and stability. The presence of a chloro-substituted pyrimidine moiety contributes to its potential biological activity, particularly in medicinal chemistry, where such compounds may exhibit properties relevant to drug development. The compound's structure suggests it may interact with biological targets, possibly influencing pathways related to amino acid metabolism or receptor modulation. Its chirality, indicated by the (S) designation, implies that it may exhibit different pharmacological effects compared to its enantiomer. Additionally, the compound's CAS number, 1289585-01-8, allows for precise identification in chemical databases, facilitating research and development efforts. Overall, this compound represents a class of molecules that may have significant implications in therapeutic applications.
Formula:C13H19ClN4O2
Synonyms:- 1-Pyrrolidinecarboxylic acid, 3-[(6-chloro-4-pyrimidinyl)amino]-, 1,1-dimethylethyl ester, (3S)-
- (S)-3-(6-Chloro-pyrimidin-4-ylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester
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(S)-tert-Butyl 3-((6-chloropyrimidin-4-yl)amino)pyrrolidine-1-carboxylate
CAS:Formula:C13H19ClN4O2Molecular weight:298.7686
