145678-68-8 Usage
Description
(S)-1-Methylpiperidine-3-carboxylic acid, also known as (S)-MP3CA, is a chiral chemical compound belonging to the class of piperidine carboxylic acids. It is the S enantiomer of the compound and has been studied for its potential pharmaceutical applications, particularly in the development of antipsychotic and analgesic medications. Its unique structure and chemical properties make it a promising candidate for therapeutic effects, and ongoing research is exploring its pharmacological properties and potential applications in the medical field.
Uses
Used in Pharmaceutical Industry:
(S)-1-Methylpiperidine-3-carboxylic acid is used as a key compound for the development of antipsychotic and analgesic medications due to its potential therapeutic effects and unique chemical properties.
Used in Drug Development:
(S)-MP3CA is utilized as a promising candidate in drug development, as its structure and properties make it suitable for creating new medications with potential applications in various medical fields.
Used in Research and Development:
(S)-1-Methylpiperidine-3-carboxylic acid is employed as a subject of ongoing research to explore its pharmacological properties and determine its potential applications in the medical field, with a focus on antipsychotic and analgesic medications.
Check Digit Verification of cas no
The CAS Registry Mumber 145678-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,7 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145678-68:
(8*1)+(7*4)+(6*5)+(5*6)+(4*7)+(3*8)+(2*6)+(1*8)=168
168 % 10 = 8
So 145678-68-8 is a valid CAS Registry Number.
145678-68-8Relevant articles and documents
Enantioselective hydrogenation of arecaidine over cinchona alkaloid-modified palladium catalyst: A novel route to enantioenriched nipecotic acid derivatives
Szollosi, Gyoergy,Szori, Kornel,Bartok, Mihaly
, p. 349 - 352 (2008)
The hydrogenation of N-methyl-3,4-dehydronipecotic acid (arecaidine) over Pd/Al2O3 catalyst in presence of cinchona alkaloids and benzylamine additive results in the quantitative formation of N-methylnipecotic acid in good (up to 60%) optical purity. The reaction is a novel example of the efficient use of chirally modified heterogeneous metal catalysts allowing the preparation of enantioenriched N-heterocyclic carboxylic acids.
