3494-04-0 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(1-Isobutyl-3-methyl-1-butenyl)pyrrolidine is used as a key intermediate in the synthesis of various pharmaceuticals due to its unique structural features and reactivity. Its ability to be modified and incorporated into more complex molecules makes it a valuable component in drug development.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
In the field of organic chemistry, 1-(1-Isobutyl-3-methyl-1-butenyl)pyrrolidine is used as a chiral auxiliary to induce stereoselectivity in asymmetric synthesis. This application is crucial for the production of enantiomerically pure compounds, which are essential in the pharmaceutical industry to ensure the desired biological activity and minimize potential side effects.
Used in Neuroprotective Agent Research:
1-(1-Isobutyl-3-methyl-1-butenyl)pyrrolidine has been studied for its potential pharmacological properties, particularly as a neuroprotective agent. Its use in this area is focused on developing treatments for neurological disorders and conditions where neuroprotection is a critical factor in disease management and prevention.
Overall, 1-(1-Isobutyl-3-methyl-1-butenyl)pyrrolidine is a versatile chemical with a wide range of potential applications in various fields, making it a valuable compound for researchers and industry professionals.
Check Digit Verification of cas no
The CAS Registry Mumber 3494-04-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3494-04:
(6*3)+(5*4)+(4*9)+(3*4)+(2*0)+(1*4)=90
90 % 10 = 0
So 3494-04-0 is a valid CAS Registry Number.
3494-04-0Relevant academic research and scientific papers
Optimum Conditions for Enamine Synthesis by an Improved Titanium Tetrachloride Procedure
Carlson, Rolf,Nilsson, Asa,Stroemqvist, Mats
, p. 7 - 14 (2007/10/02)
A modified procedure for enamine synthesis which results in shorter times and increased yield has been developed.Optimum conditions for the synthesis have been obtained from a series of eight different acyclic ketones with three different amines.The optimum conditions were determined either by response surface methodologgy or by simplex technique.In view of the results some consideration of the mechanism is briefly discussed.
