3289-39-2 Usage
Uses
Used in Medicinal Chemistry:
6-CHLORO-2-(1-PYRROLIDINYL)-4-PYRIMIDINAMINE is used as a compound of interest in medicinal chemistry for its potential to interact with biological targets, which may lead to the development of new pharmaceuticals.
Used in Pharmacology Research:
In the field of pharmacology, 6-CHLORO-2-(1-PYRROLIDINYL)-4-PYRIMIDINAMINE is utilized for research purposes to explore its potential pharmaceutical activity and to understand its mechanisms of action.
Further research and studies on the properties and uses of 6-CHLORO-2-(1-PYRROLIDINYL)-4-PYRIMIDINAMINE are essential to fully comprehend its potential benefits and risks, ensuring its safe and effective application in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 3289-39-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3289-39:
(6*3)+(5*2)+(4*8)+(3*9)+(2*3)+(1*9)=102
102 % 10 = 2
So 3289-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H11ClN4/c9-6-5-7(10)12-8(11-6)13-3-1-2-4-13/h5H,1-4H2,(H2,10,11,12)
3289-39-2Relevant academic research and scientific papers
Triamino pyrimidines and pyridines as histamine H4 receptor modulators
Meduna, Steven P.,Savall, Brad M.,Cai, Hui,Edwards, James P.,Thurmond, Robin L.,McGovern, Patricia M.
scheme or table, p. 3113 - 3116 (2011/06/26)
Two series of triamino pyrimidines and a series of triamino pyridines have been synthesized and their structure-activity relationships evaluated for activity at the H4 receptor in competitive binding and functional assays. Small structural changes in these three hetereoaromatic cores influenced the functional activity of these compounds.
A practical strategy for the synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines
Li, Chaomin,Rosenau, Andrew
experimental part, p. 5888 - 5893 (2010/01/18)
Starting from commercially available 4-amino-2,6-dichloropyrimidine, a practical four steps synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines was developed. This strategy could introduce a diverse set of secondary amines and arylamines to displac
