80681-19-2 Usage
Uses
Used in Pharmaceutical Research:
3-propyl-3H-purin-6-amine is used as a research compound for investigating its potential role in nucleic acid metabolism. Its unique structure and properties make it a valuable tool in the study of purine-related biological processes and mechanisms.
Used in Drug Development:
As a derivative of adenine, 3-propyl-3H-purin-6-amine is used as a lead compound in the development of new therapeutic agents. Its potential biological activities suggest that it could be a precursor to drugs targeting specific diseases or conditions related to nucleic acid metabolism.
Used in Biotechnology Applications:
3-propyl-3H-purin-6-amine is utilized in biotechnological applications to explore its interactions with nucleic acids and proteins. This can lead to the development of novel techniques or products in genetic engineering, diagnostics, or therapeutics.
Used in Academic Research:
In academic settings, 3-propyl-3H-purin-6-amine serves as a subject of study for understanding the fundamental aspects of purine chemistry, its interactions with biological systems, and its potential implications in various biological pathways.
Each of these uses underscores the versatility and importance of 3-propyl-3H-purin-6-amine in advancing scientific knowledge and potentially contributing to the development of new medical treatments and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 80681-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,8 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80681-19:
(7*8)+(6*0)+(5*6)+(4*8)+(3*1)+(2*1)+(1*9)=132
132 % 10 = 2
So 80681-19-2 is a valid CAS Registry Number.
80681-19-2Relevant academic research and scientific papers
Heterocyclic Ambident Nucleophiles. III* The Alkylation of Sodium Adenide
Rasmussen, Malcolm,Hope, Janet M.
, p. 525 - 534 (2007/10/02)
The alkylation of sodium adenide in HCONMe2 (30 deg) with various alkylating agents was analysed by 1H n.m.r. spectroscopy.Widely varying N3:N7:N9 alkylation patterns were observed, depending on the alkylating agent.These patterns are interpreted in terms of the electrostatic, thermodynamic and steric factors involved in the different SN2 transition states appropriate to each alkylating agent.Hydrogen bonding association between the 6-amino group and certain carbonyl containing alkylating agents is proposed to explain the enhancedN7-alkylation in some cases.Support for this latter proposal was obtain from a comparison of the adenine alkylation results with the corresponding alkylation patterns of 6-pivaloylamino- and 6-chloro-purine.
