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37761 Fluka

2,3-Dihydroxynaphthalene

technical, ≥90% (HPLC)

Synonym: 2,3-Naphthalenediol

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Properties

Related Categories Building Blocks, Chemical Synthesis, Organic Building Blocks, Oxygen Compounds, Polyols More...
grade   technical
assay   ≥90% (HPLC)
mp   161-165 °C(lit.)
  161-165 °C
Gene Information   human ... BAD(572)

Description

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Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
WGK Germany 
3
RTECS 
QJ4750000

Protocols & Articles

Peer-Reviewed Papers

References

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Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides. Mårten Jacobsson et al J. Med. Chem. 49, 1932-8, (2006)

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Reactions of linoleic acid peroxyl radicals with phenolic antioxidants: a pulse radiolysis study. Erben-Russ M, Bors W, and Saran M Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 52(3), 393-412, (1987)

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Hydrolytic metal with a hydrophobic periphery: titanium(IV) complexes of naphthalene-2,3-diolate and interactions with serum albumin. Tinoco AD, Eames EV, Incarvito CD, et al. Inorg. Chem. 47(18), 8380-90, (2008)

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A novel "pro-sensitizer" based sensing of enzymes using Tb(III) luminescence in a hydrogel matrix. Bhowmik S and Maitra U Chem. Commun. (Camb.) 48(38), 4624-6, (2012)

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The multidrug efflux regulator TtgV recognizes a wide range of structurally different effectors in solution and complexed with target DNA: evidence from isothermal titration calorimetry. Guazzaroni ME, Krell T, Felipe A, et al. J. Biol. Chem. 280(21), 20887-93, (2005)

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Regulation of rat liver phenylalanine hydroxylase. Kinetic properties of the enzyme's iron and enzyme reduction site. Shiman, R., et al. J. Biol. Chem. 269, 24637, (1994)

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The syntheses and characterizations of molybdenum(VI) complexes with catechol and 2,3-dihydroxynaphthalene, and the structure-effect relationship in their in vitro anticancer activities. Feng J, Lu XM, Wang G, et al. Dalton Trans. 41(28), 8697-702, (2012)

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Redox cycling by cytochrome P-450. Besse P, Modi S, Boyle JM, et al. Biochem. Soc. Trans. 25(4), S579, (1997)

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Terminal group effects on the fluorescence spectra of europium(III) nitrate complexes with a family of amide-based 2,3-dihydroxynaphthalene derivatives. Lei KW and Liu WS Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 65(1), 187-90, (2006)

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[The synthesis, 1H NMR and IR study of [(n-Bu)4N]2[Mo2O5(OC10H6O)2] and [(n-Bu)4N]2[Mo4O10 (OC10H6O)2(OCH3)2]]. Lu XM, Zhu HJ, Yuan HZ, et al. Guang Pu Xue Yu Guang Pu Fen Xi 22(1), 36-8, (2002)

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Tris(spiroborate)-Type Anionic Nanocycles Danjo, H., et al. Chem. Asian J. 7(7), 1529-32, (2012)

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Beil. 6,IV,6564

Aldrich MSDS 1, 710:C / Corp MSDS 1 (1), 1278:C / FT-IR 1 (1), 1112:B / FT-IR 2 (2), 1899:A / FT-NMR 1 (2), 312:B / IR-Spectra (3), 669:A / IR-Spectra (2), 597:B / NMR-Reference 2 (1), 911:C / RegBook 1 (1), 1305:E / Sax 6, 1972 / Sigma FT-IR 1 (2), 477:A / Structure Index 1, 199:D:4

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