163831-65-0 Usage
Uses
Used in Pharmaceutical Industry:
(R)-(-)-N-BENZYL-1-(1-NAPHTHYL)ETHYLAMINE HYDROCHLORIDE is used as a chiral auxiliary in asymmetric synthesis for the development of enantiomerically pure compounds, which are essential in the creation of effective and safe pharmaceuticals. (R)-(-)-N-BENZYL-1-(1-NAPHTHYL)ETHYLAMINE HYDROCHLORIDE's chiral properties allow for the synthesis of biologically active molecules with specific stereochemistry, improving drug efficacy and reducing side effects.
Used in Organic Synthesis:
(R)-(-)-N-BENZYL-1-(1-NAPHTHYL)ETHYLAMINE HYDROCHLORIDE is used as a chiral building block in the synthesis of complex organic molecules, including natural products, pharmaceuticals, and agrochemicals. Its unique structural features enable the formation of specific stereocenters, facilitating the creation of enantiomerically pure compounds with desired biological activities.
Used in Drug Development for Neurological and Psychiatric Disorders:
(R)-(-)-N-BENZYL-1-(1-NAPHTHYL)ETHYLAMINE HYDROCHLORIDE is used as a potential lead compound in the development of drugs targeting neurological and psychiatric disorders. Its unique chemical structure and chiral properties allow for the design of novel therapeutic agents with improved efficacy, selectivity, and reduced side effects, addressing unmet medical needs in these therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 163831-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,8,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 163831-65:
(8*1)+(7*6)+(6*3)+(5*8)+(4*3)+(3*1)+(2*6)+(1*5)=140
140 % 10 = 0
So 163831-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H19N.ClH/c1-15(20-14-16-8-3-2-4-9-16)18-13-7-11-17-10-5-6-12-19(17)18;/h2-13,15,20H,14H2,1H3;1H/t15-;/m1./s1
163831-65-0Relevant academic research and scientific papers
Direct reductive alkylation of amine hydrochlorides with aldehyde bisulfite adducts
Barniol-Xicota, Marta,Turcu, Andreea L.,Codony, Sandra,Escolano, Carmen,Vázquez, Santiago
supporting information, p. 2548 - 2550 (2014/05/06)
A mild procedure for the direct reaction of aromatic and aliphatic aldehyde bisulfite adducts with primary and secondary amine hydrochlorides in the presence of sodium cyanoborohydride in methanol is reported.
