7154-69-0 Usage
Uses
Used in Pharmaceutical Industry:
(R)-2-BENZYL-PENT-4-ENOIC ACID AMIDE is used as a synthetic intermediate for the development of pharmaceutical compounds. Its unique structure and potential biological activity make it a promising candidate for the creation of new drugs and therapeutic agents.
Used in Agrochemical Industry:
(R)-2-BENZYL-PENT-4-ENOIC ACID AMIDE is used as a building block in the synthesis of agrochemicals. Its potential applications in this industry include the development of new pesticides, herbicides, and other agricultural chemicals to improve crop yield and protect plants from pests and diseases.
Used in Medicinal Chemistry Research:
(R)-2-BENZYL-PENT-4-ENOIC ACID AMIDE is used as a subject of study in medicinal chemistry. Its potential biological activity and unique structure make it an interesting compound for researchers to investigate its properties and possible applications in the development of new medicines and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 7154-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7154-69:
(6*7)+(5*1)+(4*5)+(3*4)+(2*6)+(1*9)=100
100 % 10 = 0
So 7154-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO/c1-2-6-11(12(13)14)9-10-7-4-3-5-8-10/h2-5,7-8,11H,1,6,9H2,(H2,13,14)
7154-69-0Relevant academic research and scientific papers
SAR of 2-benzyl-4-aminopiperidines NK1 antagonists. Part 2. Synthesis of CGP 49823
Veenstra, Siem J.,Hauser, Kathleen,Schilling, Walter,Betschart, Claudia,Ofner, Silvio
, p. 3029 - 3034 (2007/10/03)
CGP 49823 is a potent NK1 antagonist which is centrally active after oral administration. The SAR of the C-2 substituent was investigated with respect to the affinity to the NK1 receptor. A practical synthesis of CGP 49823, suitable for scale-up, was developed. The key-step, a tandem acyliminium ion cyclization/Ritter reaction, gave trans-2-benzyl-4-acetamido-piperidines with high diastereoselectivity.
