19615-30-6 Usage
Uses
Used in Pharmaceutical Industry:
PIPERIDIN-2-YL-ACETIC ACID HYDROCHLORIDE is used as a reactant for the synthesis of enantiopure piperidine-based β-amino esters via a chemoenzymatic approach. This application is crucial in the development of novel drugs with improved selectivity and reduced side effects, as enantiopure compounds exhibit specific biological activities.
Used in Chemical Synthesis:
In the chemical synthesis industry, PIPERIDIN-2-YL-ACETIC ACID HYDROCHLORIDE is used as a reactant for the preparation of various bioactive molecules and pharmaceutical intermediates. Its versatile structure allows for further functionalization and modification, making it a valuable component in the synthesis of complex organic molecules.
Used in Enzymatic Esterification:
PIPERIDIN-2-YL-ACETIC ACID HYDROCHLORIDE is also employed in enzymatic esterification processes, where it can be converted into ester derivatives. These esters can be used as intermediates in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals, showcasing the compound's versatility in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19615-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19615-30:
(7*1)+(6*9)+(5*6)+(4*1)+(3*5)+(2*3)+(1*0)=116
116 % 10 = 6
So 19615-30-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2.ClH/c9-7(10)5-6-3-1-2-4-8-6;/h6,8H,1-5H2,(H,9,10);1H
19615-30-6Relevant academic research and scientific papers
SUBSTITUTED SULFONAMIDE DERIVATIVES
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Page/Page column 92, (2009/11/29)
The invention relates to substituted sulfonamide derivatives, processes for the preparation thereof, medicaments containing these compounds and the use of substituted sulfonamide derivatives for the preparation of medicaments.
Chemoenzymatic approach to enantiopure piperidine-based β-amino esters in organic solvents
Liljeblad, Arto,Kavenius, Hanna-Maija,Taehtinen, Petri,Kanerva, Liisa T.
, p. 181 - 191 (2007/10/03)
This research concentrates on the enantioselectivities of lipase-catalysed reactions with methyl esters of 2-piperidylacetic acid and 3-piperidinecarboxylic acid derivatives. N-Acetylated 2-piperidylacetic acid methyl ester displayed good enantioselectivi
Electrophilic Amidoalkylation of C-H Acidic Compounds with Cyclic N-Formylimmonium Precursors
Eberson, Lennart,Malmberg, Mats,Nyberg, Klas
, p. 555 - 566 (2007/10/02)
C-H acidic compounds, such as esters of malonic acid, substituted malonic acids, 2-oxocyclopentanecarboxylic acid and acetoacetic acid and in some cases monocarbonyl compounds, e.g. acetone and cyclopentanone, react with cyclic N-formyl-N-α-methoxyamines,
