61571-27-5 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
Imidazo[1,2-a]pyrimidin-2-yl-acetic acidethylester is used as a research compound for its potential biological activities. It is being studied for its potential as an anticancer agent, as well as for its anti-inflammatory and analgesic properties.
Used in Anticancer Applications:
Imidazo[1,2-a]pyrimidin-2-yl-acetic acidethylester is used as an anticancer agent, as it has been studied for its potential to target and treat cancer cells. Its specific mechanism of action and efficacy against various types of cancer are currently under investigation.
Used in Anti-inflammatory and Analgesic Applications:
Imidazo[1,2-a]pyrimidin-2-yl-acetic acidethylester is used as an anti-inflammatory and analgesic agent, as it has been studied for its potential to reduce inflammation and alleviate pain. Its effectiveness and safety in these applications are being researched.
Used in Medicine and Biotechnology:
Imidazo[1,2-a]pyrimidin-2-yl-acetic acidethylester is used in various fields of medicine and biotechnology, given its potential applications in drug development and treatment of various conditions. Its versatility and biological activities make it a promising candidate for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 61571-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,7 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61571-27:
(7*6)+(6*1)+(5*5)+(4*7)+(3*1)+(2*2)+(1*7)=115
115 % 10 = 5
So 61571-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O2/c1-2-15-9(14)6-8-7-13-5-3-4-11-10(13)12-8/h3-5,7H,2,6H2,1H3
61571-27-5Relevant academic research and scientific papers
Synthesis, crystal structures and spectral characterization of imidazo[1,2-a]pyrimidin-2-yl-acetic acid and related analog with imidazo[2,1-b]thiazole ring
Dylong, Agnieszka,Goldeman, Waldemar,Sowa, Micha?,?lepokura, Katarzyna,Drozdzewski, Piotr,Matczak-Jon, Ewa
, p. 153 - 163 (2016/04/06)
Imidazo[1,2-a]pyrimidin-2-yl-acetic acid (HIPM-2-ac) and its analog with imidazo[2,1-b]thiazole ring (HITZ-6-ac) were synthesized and structurally characterized by single-crystal X-ray diffraction corroborated with calculations of Hirshfeld surfaces, which provided detailed insight into intermolecular interactions constituting both crystals. The IR and Raman spectra of HIPM-2-ac and HITZ-6-ac were recorded and interpreted in details with the aid of Density Functional Theory (DFT) calculations and Potential Energy Distribution (PED) analysis of computed normal vibrations. Special attention was paid on hydroxyl and methylene groups involved in hydrogen bonds, which vibrations were monitored by H/D substitution. Recrystallization of parent compounds from deuterium oxide (D2O) solutions resulted in deuteration of their carboxylic OH groups and almost complete deuteration of HIPM-2-ac methylene group. The latter phenomenon is clearly reflected in the vibrational spectra and confirmed by 1H NMR experiments in solution.
