CAS 183483-15-0
:4-(8-Chloro-5,6-dihydro-3-hydroxy-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylic Acid Ethyl Ester
Description:
4-(8-Chloro-5,6-dihydro-3-hydroxy-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylic Acid Ethyl Ester, with CAS number 183483-15-0, is a chemical compound characterized by its complex structure, which includes a piperidine ring and a benzo[5,6]cyclohepta[1,2-b]pyridine moiety. This compound features a chloro substituent and a hydroxyl group, contributing to its potential biological activity. The presence of the ethyl ester functional group suggests that it may exhibit lipophilic properties, which can influence its solubility and permeability in biological systems. The compound's unique structural features may allow it to interact with specific biological targets, making it of interest in medicinal chemistry and pharmacology. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its properties could be further explored through various analytical methods, including NMR, mass spectrometry, and chromatography. Overall, this compound represents a class of molecules that may have therapeutic potential, warranting further investigation into its biological effects and mechanisms of action.
Formula:C22H23ClN2O3
InChI:InChI=1/C22H23ClN2O3/c1-2-28-22(27)25-9-7-14(8-10-25)20-19-6-5-17(23)11-15(19)3-4-16-12-18(26)13-24-21(16)20/h5-6,11-13,26H,2-4,7-10H2,1H3
SMILES:CCOC(=O)N1CCC(=C2c3ccc(cc3CCc3cc(cnc23)O)Cl)CC1
Synonyms:- 3-Hydroxy Loratadine
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Found 5 products.
Ethyl 4-(8-chloro-5,6-dihydro-3-hydroxy-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylate
CAS:Formula:C22H23ClN2O3Color and Shape:SolidMolecular weight:398.88263-Hydroxy Loratadine
CAS:Controlled Product<p>Applications An intermediate for the preparation of 3-Hydroxy Desloratadine.<br></p>Formula:C22H23ClN2O3Color and Shape:NeatMolecular weight:398.883-Hydroxy loratadine
CAS:<p>Loratadine is a nonsteroidal antihistamine that competitively blocks histamine H1 receptors in the brain, which decreases the allergic response. It also has glucuronide metabolites, which are eliminated by the kidney and can be measured in the plasma concentration. Loratadine's time-dependent effect on histamine release is due to its ability to block histamine H1 receptors for up to 12 hours after administration. Loratadine has been shown to have an antagonistic effect on clopidogrel, meaning it prevents the drug from working properly by blocking its action at the H1 receptor. This interaction could result in increased risk of adverse events, such as heart attack or stroke.</p>Formula:C22H23ClN2O3Purity:Min. 95%Molecular weight:398.88 g/mol




