174543-82-9 Usage
Uses
Used in Pharmaceutical Synthesis:
Methyl 1-Cbz-3-Methylpiperidine-3-carboxylate is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and the presence of the carbobenzyloxy protecting group make it a versatile building block for creating complex organic molecules with potential therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, Methyl 1-Cbz-3-Methylpiperidine-3-carboxylate serves as a crucial component in the development of new synthetic routes and methodologies. Its reactivity and the ability to protect the amine group allow chemists to perform a wide range of reactions, leading to the formation of diverse chemical entities with potential applications in various industries.
Used in Biological Research:
Methyl 1-Cbz-3-Methylpiperidine-3-carboxylate is utilized in biological research to investigate its biological activities and potential pharmacological properties. Its unique structure and the presence of the carbobenzyloxy group make it an interesting candidate for studying its interactions with biological targets, such as enzymes, receptors, or other macromolecules, which could lead to the discovery of new therapeutic agents or drug leads.
Used in Drug Development:
In the pharmaceutical industry, Methyl 1-Cbz-3-Methylpiperidine-3-carboxylate is employed as a starting material or a building block in the development of new drugs. Its potential biological activities and pharmacological properties make it a promising candidate for the creation of innovative therapeutic agents that can address unmet medical needs or improve the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 174543-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,5,4 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 174543-82:
(8*1)+(7*7)+(6*4)+(5*5)+(4*4)+(3*3)+(2*8)+(1*2)=149
149 % 10 = 9
So 174543-82-9 is a valid CAS Registry Number.
174543-82-9Relevant academic research and scientific papers
On the Ritter reaction of cyclic hydroxyamines: Synthesis of conformationally-restricted reduced amide dipeptide isosteres
Taylor, G. Mark,Baker, Stewart J.,Gedney, Andrea,Pearson, David J.,Sibley, Graham E. M.
, p. 1297 - 1300 (2007/10/03)
The Ritter reactions of 3-alkyl-3-hydroxyazetidine or -piperidine derivatives give low yields of the desired products, whereas the 3-alkyl-3-hydroxy-pyrrolidine and 4-alkyl-4-hydroxy-piperidine derivatives react smoothly to give the corresponding acetamides. An alternative route to 3-acylamino-3-alkylpiperidines, which were designed as conformationally-restricted reduced amide dipeptide isosteres, was devised from nipecotic acid vai a Hofmann rearrangement.
