749192-64-1 Usage
General Description
(3R,4R)-Ethyl 4-phenylpiperidine-3-carboxylate is a chemical compound with the molecular formula C16H21NO2. It is a piperidine derivative, containing an ethyl ester group and a phenyl ring. (3R,4R)-Ethyl 4-phenylpiperidine-3-carboxylate is commonly used in the synthesis of pharmaceuticals and research chemicals. It may also have potential application as a psychoactive substance or as a precursor for the synthesis of other psychoactive compounds. Its stereochemical configuration, with the (3R,4R) configuration, is important for its biological activity and chemical reactivity. Overall, (3R,4R)-Ethyl 4-phenylpiperidine-3-carboxylate is an important compound with diverse potential applications in the field of chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 749192-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,9,1,9 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 749192-64:
(8*7)+(7*4)+(6*9)+(5*1)+(4*9)+(3*2)+(2*6)+(1*4)=201
201 % 10 = 1
So 749192-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO2/c1-2-17-14(16)13-10-15-9-8-12(13)11-6-4-3-5-7-11/h3-7,12-13,15H,2,8-10H2,1H3/t12-,13-/m0/s1
749192-64-1Relevant articles and documents
Synthesis and Discovery of Arylpiperidinylquinazolines: New Inhibitors of the Vesicular Monoamine Transporter
Provencher, Brian A.,Eshleman, Amy J.,Johnson, Robert A.,Shi, Xiao,Kryatova, Olga,Nelson, Jared,Tian, Jianhua,Gonzalez, Mario,Meltzer, Peter C.,Janowsky, Aaron
, p. 9121 - 9131 (2018/10/20)
Methamphetamine, a human vesicular monoamine transporter 2 (VMAT2) substrate, releases dopamine, serotonin, and norepinephrine from vesicles into the cytosol of presynaptic neurons and induces reverse transport by the monoamine transporters to increase ex
Derives alkyles et aryles de l'acide nipecotique: synthese et appreciation de l'activite inhibitrice de la capture du GABA en fonction de parametres conformationnels et de biodisponibilite
Lapuyade, Gerard,Schlewer, Gilbert,N'Goka, Victor,Vernieres, Jean-Claude,Chambon, Jean-Pierre,et al.
, p. 383 - 392 (2007/10/02)
Alkyl and aryl derivatives of nipecotic acid: synthesis and inhibition of GABA uptake as a function of conformational parameters and bioavailability.Analogs of nipecotic acid, substituted at positions 2, 3, 4, 5, or 6 with a methyl or phenyl group were pr
