5069-82-9 Usage
Uses
Used in Biochemical Research:
6-(BUTYLTHIO)-PURINE is used as a research tool for studying the structure and function of adenosine receptors, which are important in various physiological processes.
Used in Pharmacological Studies:
6-(BUTYLTHIO)-PURINE is used as a compound in pharmacological research to explore its potential effects on different biological systems and to understand its interaction with adenosine receptors, which could lead to the development of new therapeutic agents.
Used in Drug Development:
6-(BUTYLTHIO)-PURINE is used as a lead compound in the development of novel drugs targeting adenosine receptors for the treatment of various medical conditions, given its unique chemical structure and potential pharmacological activity.
Used in the Pharmaceutical Industry:
6-(BUTYLTHIO)-PURINE is used as a key component in the synthesis of new drug candidates, particularly those aimed at modulating adenosine receptor activity for therapeutic purposes.
Used in Academic Research:
6-(BUTYLTHIO)-PURINE is used as a subject of study in academic research to further elucidate its biological effects and to identify new applications in medicine and biology.
Used in Preclinical Testing:
6-(BUTYLTHIO)-PURINE is used in preclinical models to assess its safety, efficacy, and pharmacokinetics, which are crucial steps in the drug development process before moving to clinical trials.
Check Digit Verification of cas no
The CAS Registry Mumber 5069-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5069-82:
(6*5)+(5*0)+(4*6)+(3*9)+(2*8)+(1*2)=99
99 % 10 = 9
So 5069-82-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N4S/c1-2-3-4-14-9-7-8(11-5-10-7)12-6-13-9/h5-7H,2-4H2,1H3
5069-82-9Relevant academic research and scientific papers
Modification of thionucleobases in ionic liquids
Hu, Xiaomei,Zhang, Bixian,Dong, Shijia,Gao, Yunfei
, (2015/02/19)
A simple method was established for the preparation of thio-substituted thionucleobases using room temperature ionic liquids (RTILs) such as 1-butyl-3-methylimidazolium trifluoroacetate [BMIM]+[CF3COO]- and 1-methoxyethyl-3-methylimidazolium trifluoroacetate [MeOEtMIM]+[CF3COO]- as solvents and catalysts without any other catalyst. These reactions proceeded efficiently in RTILs with excellent yield of products. RTILs can be recycled and reused effectively without further purification.
A New Method for the Synthesis of Heterocyclic S-Alkyl Thiolactams
Jackman, Dennis E.,Westphal, Dietmar B.
, p. 1134 - 1136 (2007/10/02)
The reaction of S-substituted heterocyclic thiolactams with thiols is described.In some cases, rearrangement or tricyclic products were produced instead of the compounds expected from simple alkylthiol displacement.
