167170-23-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl N-Cbz-2-piperidineacetate is used as an intermediate in the pharmaceutical industry for the synthesis of piperidine-based compounds. Its role is crucial in the preparation of various medications, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, Ethyl N-Cbz-2-piperidineacetate serves as a valuable component in the synthesis of complex organic molecules. Its structural properties make it suitable for use in the creation of a wide range of organic compounds.
Used in Drug Discovery Research:
Ethyl N-Cbz-2-piperidineacetate is utilized in drug discovery research to explore its potential in the development of new pharmaceutical agents. Its unique chemical properties allow researchers to investigate its interactions with biological targets, which may lead to the discovery of novel treatments and medications.
Check Digit Verification of cas no
The CAS Registry Mumber 167170-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,1,7 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 167170-23:
(8*1)+(7*6)+(6*7)+(5*1)+(4*7)+(3*0)+(2*2)+(1*3)=132
132 % 10 = 2
So 167170-23-2 is a valid CAS Registry Number.
167170-23-2Relevant academic research and scientific papers
Synthesis of optically active 2-piperidylglycine
Chung, Hyun-Kyu,Kim, Hyung-Woo,Chung, Kyoo-Hyun
, p. 2983 - 2989 (2007/10/03)
Both chiral threo- and erythro-2-piperidylglycines were synthesized from racemic 2-[(N-benzyloxycarbonyl)piperidin-2-yl]ethanoic acid. (4S,5S)-4- Methyl-5-phenyl-2-oxa-zolidinone was used as a chiral auxiliary in the resolution and azidation.
Azacycle Synthesis via Radical Cyclization of β-Aminoacrylates.
Lee, Eun,Kang, Tae Seop,Joo, Beom Jun,Tae, Jin Sung,Li, Kap Sok,Chung, Cheol Keun
, p. 417 - 420 (2007/10/02)
(Pyrrolidine)- and (piperidine)acetates are efficiently synthesized via radical cyclization of β-aminoacrylates.
