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PYRENESULFONYL CHLORIDE

Physical Form Bright yellow crystals Orange [Pg.350]

Solubility Soluble in acetonitrile, chloroform, N,N-dimethylformamide, methanol, xylenes [Pg.350]

Vollmann, H. Becker, H. Corell, M. Streeck, H. Pyrene and its derivatives. Justus Liebigs Ann. Chem. [Pg.350]

Hemgesherg, M. Schuetz, S. Mueller, C. Schloerholz, M. Latzel, H. Sun, Y. Ziegler, C. Thiel, W. R. Ultra-fast photo-patterning of hydroxamic acid layers adsorbed on TiAlN The challenge of modeling thermally induced desorption. Appl. Surf. Sci. 2012, 259,406 15. [Pg.350]

Salameh, A. S. Castner, E. W., Jr., Wishart, J. K Isied, S. S. Conformational analysis of the electron-transfer kinetics across oligoproline peptides using N,N-dimethyl-l,4-benzenediamine donors and pyrene-1-sulfonyl acceptors. J. Phys. Chem. B2007, 111, 6878-6886. [Pg.350]


Min, J. Z. Kurihara, T Hirata, A. Toyo oka, T. Inagaki, S. Identification of A-linked oligosaccharide labeled with 1-pyrenesulfonyl chloride by quadrupole time-of-flight tandem mass spectrometry after separation by micro- and nanoflow liquid chromatography. Biomed. Chromatogr. 2009, 23, 912-921. [Pg.350]

Pyrenesulfonyl chloride 1,3,6,8-Pyrenetetrasulfonic acid tetrasodium salt N-( 1 -Pyrenyl)iodoacetamide A-(l -Pyrenyl)maleimide... [Pg.443]


See other pages where PYRENESULFONYL CHLORIDE is mentioned: [Pg.35]    [Pg.350]    [Pg.350]    [Pg.350]    [Pg.350]    [Pg.351]    [Pg.427]    [Pg.35]    [Pg.350]    [Pg.350]    [Pg.350]    [Pg.350]    [Pg.351]    [Pg.427]   


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