378750-49-3 Usage
Uses
Used in Pharmaceutical Research and Development:
2,4(1H,3H)-Pyrimidinedione, 3-benzoyl-1-(3-bromo-1-methylpropyl)is used as a chemical intermediate for the synthesis of new drugs. Its unique structure and functional groups may contribute to the development of novel therapeutic agents with potential biological activity.
Used in Chemical Synthesis:
2,4(1H,3H)-Pyrimidinedione, 3-benzoyl-1-(3-bromo-1-methylpropyl)can be used as a building block for the synthesis of other chemical compounds. Its benzoyl and 3-bromo-1-methylpropyl groups may allow for further chemical reactions and modifications, leading to the creation of new molecules with specific properties and applications.
Used in Drug Discovery:
2,4(1H,3H)-Pyrimidinedione, 3-benzoyl-1-(3-bromo-1-methylpropyl)may have potential biological activity, making it a candidate for drug discovery. Its unique structure could be explored for interactions with biological targets, such as enzymes, receptors, or other proteins, potentially leading to the development of new therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4(1H,3H)-Pyrimidinedione, 3-benzoyl-1-(3-bromo-1-methylpropyl)- can be studied to understand its structure-activity relationships and optimize its properties for specific therapeutic applications. Its unique functional groups and potential biological activity make it a valuable compound for further exploration and optimization in the development of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 378750-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,8,7,5 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 378750-49:
(8*3)+(7*7)+(6*8)+(5*7)+(4*5)+(3*0)+(2*4)+(1*9)=193
193 % 10 = 3
So 378750-49-3 is a valid CAS Registry Number.
378750-49-3Relevant academic research and scientific papers
Stereoselective construction of the azabicyclic core applicable to the biologically important polyguanidinium alkaloids batzelladine A and D using a free radical cyclization
Evans,Manangan, Thara
, p. 6637 - 6640 (2007/10/03)
The intramolecular addition of the free radical derived from the alkyl bromide 13 provides an expeditious and stereoselective approach to the azabicyclic core 14, which is applicable to the biologically important polyguanidinium alkaloids batzelladine A (1) and D (2).
