27345-54-6 Usage
Uses
Used in Pharmaceutical Industry:
N-(9-benzyl-9H-purin-6-yl)acetamide is used as a potential therapeutic agent for various diseases due to its structural similarity to purine nucleosides, which are essential in DNA and RNA synthesis. Its potential applications may include the treatment of genetic disorders, cancer, and other diseases where modulation of nucleic acid synthesis could be beneficial.
Used in Medicinal Chemistry Research:
N-(9-benzyl-9H-purin-6-yl)acetamide serves as a valuable compound in medicinal chemistry research, where it can be studied for its potential biological activities and pharmacological properties. Researchers may investigate its interactions with enzymes, receptors, or other biological targets to understand its mechanism of action and explore its potential as a lead compound in drug development.
Used in Drug Development:
As a derivative of purine and acetamide, N-(9-benzyl-9H-purin-6-yl)acetamide may be utilized in drug development to create novel therapeutic agents. Its unique structure could be optimized through chemical modifications to enhance its potency, selectivity, and pharmacokinetic properties, ultimately leading to the development of new drugs with improved therapeutic efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 27345-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,4 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27345-54:
(7*2)+(6*7)+(5*3)+(4*4)+(3*5)+(2*5)+(1*4)=116
116 % 10 = 6
So 27345-54-6 is a valid CAS Registry Number.
27345-54-6Relevant academic research and scientific papers
The Prominent Effect of N6-Acyl Groups on the Reactivity of 9-Substituted Adenines: A New Method for the Chemical Modification of Adenines
Maki, Yoshifumi,Kameyama, Keiji,Suzuki, Mikio,Sako, Magoichi,Hirota, Kosaku
, p. 3601 - 3654 (2007/10/02)
The effect of various N6-substituents on the C(8)-hydrogen exchange of 9-substituted adenines has been estimated.The kinetic data clearly demonstrate that the N6-acyl groups significantly accelerate the C(8)-hydrogen exchange.This fa
