Keywords
meso-sulfophenyloxy dyes
N-acylsulfonamides
acetylation
cyanine dyes
electroneutral dyes
fluorescently labeled nucleotides
heptamethine dyes
sulfonamides
Abstract
A novel electroneutral rigid meso-sulfophenyloxy substituted heptamethine dye was synthesized in six steps. Selective derivatization of one sulfonamide group with octanedioic acid introduced the carboxy end group attached through the hexamethylene linker, which provided the dye solubility in water. Absorbance of the dye in the near infrared region makes it promising for covalent labeling of biomolecules.
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