368429-72-5 Usage
Uses
Used in Pharmaceutical Industry:
1-benzyl-5-oxo-3-pyrrolidinecarbohydrazide is used as a ligand for biological targets due to its ability to interact with various molecular entities, which is crucial for the development of new drugs and therapeutic agents.
Used in Cancer Research:
In cancer research, 1-benzyl-5-oxo-3-pyrrolidinecarbohydrazide is utilized as a potential lead compound for the development of anticancer drugs, given its capacity to engage with biological targets that are implicated in cancer progression and cell survival.
Used in Neurological Disorders Research:
For neurological disorders, 1-benzyl-5-oxo-3-pyrrolidinecarbohydrazide is employed as a chemical probe to investigate the molecular mechanisms underlying these conditions, potentially leading to the discovery of novel treatments.
Used in Organic Synthesis:
In the field of organic synthesis, 1-benzyl-5-oxo-3-pyrrolidinecarbohydrazide is used as a building block or intermediate for the creation of new compounds with tailored biological activities, contributing to the advancement of chemical libraries for drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 368429-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,8,4,2 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 368429-72:
(8*3)+(7*6)+(6*8)+(5*4)+(4*2)+(3*9)+(2*7)+(1*2)=185
185 % 10 = 5
So 368429-72-5 is a valid CAS Registry Number.
368429-72-5Relevant academic research and scientific papers
A convenient route to 1-benzyl 3-aminopyrrolidine and 3-aminopiperidine
Jean, Ludovic,Baglin, Isabelle,Rouden, Jacques,Maddaluno, Jacques,Lasne, Marie-Claire
, p. 5645 - 5649 (2007/10/03)
1-Benzyl 3-aminopyrrolidine 1 and 1-benzyl 3-aminopiperidine 2 were prepared rapidly mainly in aqueous conditions in 55 and 75% yields, respectively, on a multi-gram scale starting from inexpensive and commercially available starting materials. The key step involved the Curtius rearrangement mediated by sodium nitrite and trifluoroacetic acid of the appropriate acylhydrazides. All the reactions (except LAH reductions) were performed in water.
