N-Alkoxy-3,5-dinitro-4-aminobenzoic acid derivatives with controlled physico-chemical properties was written by Tudose, Madalina;Badea, Florin D.;Ionita, Gabriela;Maganu, Maria;Caproiu, Miron T.;Ionita, Petre;Constantinescu, Titus;Balaban, Alexandru T.. And the article was included in Structural Chemistry in 2010.HPLC of Formula: 80480-15-5 The following contents are mentioned in the article:
Starting from 4-chloro-3,5-dinitrobenzoic acid 1, compounds (N-alkoxy-3,5-dinitro-4-aminobenzoic acid esters where alkoxy stands for methoxy, carboxymethoxy, triphenylmethoxy, or corresponding amides) have been obtained, from which some are new, and for the known compounds 4-methoxyamino-3,5-dinitrobenzoic acid 2 and 4-chloro-3,5-dinitrobenzoyl chloride 6, the synthetic procedure has been improved. The new derivatives have been characterized by appropriate means (IR, UV-vis, 1H-, and 13C-NMR, fluorescence) and their properties were studied. Thus, depending on their structure, the compounds have acid properties, fluorescence and complexing properties with alk. cations. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5HPLC of Formula: 80480-15-5).
2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.HPLC of Formula: 80480-15-5
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary