Molecular structure of 1,6-Dihydroxynaphthalene, CAS Number: 575-44-0
1,6-Dihydroxynaphthalene (CAS 575-44-0)
Alternate Names:
1,6-Naphthalenediol
CAS Number:
575-44-0
Molecular Weight:
160.17
Molecular Formula:
C10H8O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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1,6-Dihydroxynaphthalene appears as a white crystalline powder, which, while being sparingly water-soluble, dissolves readily in organic solvents like acetone and benzene. As a fluorescent compound, 1,6-Dihydroxynaphthalene has been employed as a protein cross-linker and as an analytical technique for gauging naphthalene concentrations. By acting as an enzyme inhibitor, 1,6-Dihydroxynaphthalene hinders protein synthesis, specifically preventing the creation of peptide bonds within the ribosome. In scientific research, 1,6-Dihydroxynaphthalene′s versatility shines, being pivotal in chemical syntheses, exploring its biological effects, and playing roles in biosensor advancements and organic electronics.
1,6-Dihydroxynaphthalene (CAS 575-44-0) References
- Synthesis and photophysical properties of new fluorinated benzo[c]xanthene dyes as intracellular pH indicators. | Liu, J., et al. 2001. Bioorg Med Chem Lett. 11: 2903-5. PMID: 11677123
- Understanding the substrate selectivity and the product regioselectivity of Orf2-catalyzed aromatic prenylations. | Cui, G., et al. 2007. Biochemistry. 46: 1303-11. PMID: 17260959
- One-Pot Synthesis of New Symmetric and Asymmetric Xanthene Dyes. | Hilderbrand, SA. and Weissleder, R. 2007. Tetrahedron Lett. 48: 4383-4385. PMID: 19834587
- The preparation and application of functionalised synthetic oligonucleotides: III. Use of H-phosphonate derivatives of protected amino-hexanol and mercapto-propanol or -hexanol. | Sinha, ND. and Cook, RM. 1988. Nucleic Acids Res. 16: 2659-69. PMID: 3362678
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,6-Dihydroxynaphthalene, 25 g | sc-273658 | 25 g | $63.00 |