In 2019,Research Journal of Pharmaceutical, Biological and Chemical Sciences included an article by Ivanchenko, Dmytro; Romanenko, Mykola; Goloborodko, Oleksandr; Kamyshnyi, Oleksandr; Polishchuk, Natalia. HPLC of Formula: 13325-10-5. The article was titled 《Synthesis and biological activity of 8-aminosubstituted 7-(2-hydroxy-3-methylphenoxypropyl-1)-3-methylxanthine》. The information in the text is summarized as follows:
The reaction of 8-bromo-3-methylxanthine with m-ethylphenoxymethyloxirane in propanol-1 medium in the presence of N,N-dimethylbenzylamine led to formation of 8-bromo-7-(2-hydroxy-3-methylphenoxypropyl-1)-3-methylxanthine which was then interacted with amines to afford 8-aminosubstituted 7-(2-hydroxy-3-m-ethylphenoxypropyl-1)-3-methylxanthines I [R1 = H, Me, Et; R2 = Me, n-Pr, cyclohexyl, etc.]. Structures of the synthesized compounds I were proved by 1H NMR-spectroscopy. The synthesized compounds I revealed moderate to weak antibacterial and antifungal activities in concentrations 50-200 mcg/mL. The experimental process involved the reaction of 4-Aminobutan-1-ol(cas: 13325-10-5HPLC of Formula: 13325-10-5)
4-Aminobutan-1-ol(cas: 13325-10-5) is used in the synthesis of NSAIDs with anti-inflammatory properties. Also used in the synthesis of polyamine transport ligands with specificity against human cancers allowing easy access to specific cancer cells.HPLC of Formula: 13325-10-5
Referemce:
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Alcohols – Chemistry LibreTexts