4695-77-6 Usage
Uses
Used in Organic Synthesis:
Tert-butyl 1,4,5,6-tetrahydropyridine-3-carboxylate serves as a key intermediate in organic synthesis, facilitating the construction of a variety of complex organic molecules. Its unique structure allows for the development of new compounds with potential applications across different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, tert-butyl 1,4,5,6-tetrahydropyridine-3-carboxylate is utilized as a potential drug candidate. Its structural attributes make it a candidate for the development of new therapeutic agents, particularly those targeting the central nervous system or other physiological processes where pyridine-based compounds have shown efficacy.
Used in Academic Research:
Tert-butyl 1,4,5,6-tetrahydropyridine-3-carboxylate also finds application in academic research, where it is employed to explore the structure-activity relationships of pyridine-based compounds. This helps researchers understand the impact of structural modifications on the biological activity and pharmacological properties of these compounds, thereby aiding in the design of more effective drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 4695-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,9 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4695-77:
(6*4)+(5*6)+(4*9)+(3*5)+(2*7)+(1*7)=126
126 % 10 = 6
So 4695-77-6 is a valid CAS Registry Number.
4695-77-6Relevant academic research and scientific papers
A short synthesis of (±)-matrine [2]
Boiteau, Laurent,Boivin, Jean,Liard, Annie,Quiclet-Sire, Beatrice,Zard, Samir Z.
, p. 1128 - 1130 (2007/10/03)
Three different radical reactions were used in a short total synthesis of (±)-matrine (1). Two of the four six-membered rings and four new bonds were created in one radical cascade involving intermolecular addition followed by two successive cyclizations and transfer of a xanthate group.
