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5-Bromofuroic acid | CAS:585-70-6
5-Bromofuroic acid
  • Name:5-Bromofuroic acid
  • CAS:585-70-6
  • Synonyms:5-Bromo-2-furoic acid; 5-Bromo-2-furancarboxylic acid
  • Molecular Formula:C5H3BrO3
  • Molecular Weight:190.98
  • EINESC:209-559-7

Description

Properties

Melting point 189-190 ºC

Safety

SDS/MSDS S24/25

SDS

Source SDS/MSDS Samples
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Peer-Reviewed Papers
Inhibition of the transcriptional repressor LexA: Withstanding drug resistance by inhibiting the bacterial mechanisms of adaptation to antimicrobials.Pierangelo Bellio et al.Life sciences, 241, 117116-117116 (2019-12-04) Novel rhodamine dyes via Suzuki coupling of xanthone triflates with arylboroxinsCalitree, B. D.; Detty, M. R. Synlett, 89-92 (2010) An injectable and tumor-specific responsive hydrogel with tissue-adhesive and nanomedicine-releasing abilities for precise locoregional chemotherapy.Di Wu et al.Acta biomaterialia, 96, 123-136 (2019-06-28) Synthesis of a phenylboronic acid-functionalized thermosensitive block copolymer and its application in separation and purification of vicinal-diol-containing compoundsWang Y, et al. Royal Society of Chemistry Advances, 6(85), 82309-82320 (2016) Boronic acid-decorated metal-organic frameworks modified via a mixed-ligand strategy for the selective enrichment of cis-diol containing nucleosides.Ruiqi Zhang et al.Analytica chimica acta, 1106, 42-51 (2020-03-09) Selective urokinase-type plasminogen activator (uPA) inhibitors. Part 3: 1-isoquinolinylguanidines.Christopher G Barber et al.Bioorganic & medicinal chemistry letters, 14(12), 3227-3230 (2004-05-20) Heterocycles, 60, 1891-1897 (2003) Magnetic fluorescent molecularly imprinted nanoparticles for detection and separation of transferrin in human serum.Yi-Da Zhang et al.Talanta, 188, 540-545 (2018-07-22) New imidazo [1, 2-a] quinoxaline derivatives: synthesis and in vitro activity against human melanomaDeleuze-Masquefa C, et al. European Journal of Medicinal Chemistry, 44(9), 3406-3411 (2009) Identification and optimization of a novel series of indoleamine 2, 3-dioxygenase inhibitorsMarkwalder JA, et al. Bioorganic & Medicinal Chemistry Letters, 27(3), 582-585 (2017)
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