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(R)-Ethyl 2-phenyl-2-((R)-piperidin-2-yl)acetate hydrochloride

Base Information
  • Chemical Name:(R)-Ethyl 2-phenyl-2-((R)-piperidin-2-yl)acetate hydrochloride
  • CAS No.:851764-84-6
  • Molecular Formula:C15H21NO2.ClH
  • Molecular Weight:283.7940
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00464507
  • Mol file:851764-84-6.mol
(R)-Ethyl 2-phenyl-2-((R)-piperidin-2-yl)acetate hydrochloride

Synonyms:851764-84-6;(R)-Ethyl 2-phenyl-2-((R)-piperidin-2-yl)acetate hydrochloride;D-threo-Ethylphenidate Hydrochloride;d,l-threo-Ethylphenidate.HCl;ethyl (2R)-2-phenyl-2-[(2R)-piperidin-2-yl]acetate;hydrochloride;Ethylphenidate Hydrochloride;alpha-Phenyl-2-piperidineacetic acid ethyl ester hydrochloride;Methylphenidate Hydrochloride Imp. E (EP) as Hydrochloride;Methylphenidate Hydrochloride Impurity E as Hydrochloride;Methylphenidate Impurity E as Hydrochloride;ETHYL (2R)-2-PHENYL-2-[(2R)-PIPERIDIN-2-YL]ACETATE HYDROCHLORIDE;DTXSID00464507;Ethyl (2RS)-Phenyl[(2RS)-piperidin-2-yl]acetate Hydrochloride (Ethylphenidate Hydrochloride);AKOS016843401;PD048278;d,l-threo-Ethylphenidate.HCl, 1mg/ml in Ethanol;Ethyl phenyl[(2R)-piperidin-2-yl]acetate--hydrogen chloride (1/1);Ethylphenidate Hydrochloride 1.0 mg/ml in Acetonitrile (as free base);ethyl (2R)-2-phenyl-2-[(2R)-piperidin-2-yl]acetate hydrochloride

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Chemical Property of (R)-Ethyl 2-phenyl-2-((R)-piperidin-2-yl)acetate hydrochloride
Chemical Property:
  • Melting Point:224-226 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7)) 
  • PSA:38.33000 
  • LogP:3.60620 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:283.1339066
  • Heavy Atom Count:19
  • Complexity:261
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C(C1CCCCN1)C2=CC=CC=C2.Cl
  • Isomeric SMILES:CCOC(=O)[C@@H]([C@H]1CCCCN1)C2=CC=CC=C2.Cl
  • Uses The D-threo isomer of Ethylphenidate, a metabolite of Methylphenidate (M325680). D-threo-Ethylphenidate is formed by metabolic transesterification of Methylphenidate and ethanol.