169032-19-3 Usage
Chemical class
propionitriles
Structural features
contains a piperidine ring, a butyl group, a phenyl group, and a hydroxyl group
Common uses
potential drug candidate in the pharmaceutical industry, particularly as an antipsychotic or antihistamine; potential applications in the treatment of various neurological disorders and as a tool in neuroscience research; may have uses in the synthesis of other organic compounds due to its unique structural features.
Versatility
potential applications in both the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 169032-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,0,3 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 169032-19:
(8*1)+(7*6)+(6*9)+(5*0)+(4*3)+(3*2)+(2*1)+(1*9)=133
133 % 10 = 3
So 169032-19-3 is a valid CAS Registry Number.
169032-19-3Relevant academic research and scientific papers
PROCESS FOR THE PREPARATION OF FEXOFENADINE AND OF INTERMEDIATES USED THEREIN
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Page/Page column 42, (2017/05/10)
A new process for the preparation of fexofenadine and of related intermediates, which can be used in the preparation of fexofenadine, is provided.
A new synthesis of carboxyterfenadine (fexofenadine) and its bioisosteric tetrazole analogs
Di Giacomo, Barbara,Coletta, Donato,Natalini, Benedetto,Ni, Ming-Hong,Pellicciari, Roberto
, p. 600 - 610 (2007/10/03)
A new synthesis of carboxyterfenadine (4), based on the conversion of a α-halo-alkylarylketone into the corresponding substituted 2-arylalkanoic ester, is described. The enantioselective synthesis of its two bioisosteric tetrazole analogs together with preliminary biological results are reported. Copyright (C) 1999 Elsevier Science S.A.
