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9,10-Phenanthrenequinone, 95%
9,10-Phenanthrenequinone, 95%
9,10-Phenanthrenequinone, 95%
Thermo Scientific Chemicals

9,10-Phenanthrenequinone, 95%

CAS: 84-11-7 | C14H8O2 | 208.216 g/mol
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Catalog number A11762.06
also known as A11762-06
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28.65
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Quantity:
5 g
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Price (USD)
28.65
Online Exclusive
31.40
Save 2.75 (9%)
Each
Chemical Identifiers
CAS84-11-7
IUPAC Name9,10-dihydrophenanthrene-9,10-dione
Molecular FormulaC14H8O2
InChI KeyYYVYAPXYZVYDHN-UHFFFAOYSA-N
SMILESO=C1C(=O)C2=CC=CC=C2C2=CC=CC=C12
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SpecificationsSpecification SheetSpecification Sheet
Solution TestClear, orange soln(2.5% in DCM)
Appearance (Color)Orange to orange-brown
Formcrystalline powder
Assay (HPLC)>96.0%
9,10-Phenanthrenequinon may be used for high quality passivation on silicon (100) surfaces. Quinones may serve as substrates for a variety of flavoenzymes, useful fluorescent compound and quinone. Also used in dyes, as a hardener for dental restoration, for the determination of copper by spectrophotometric method, and for organic synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
9,10-Phenanthrenequinon may be used for high quality passivation on silicon (100) surfaces. Quinones may serve as substrates for a variety of flavoenzymes, useful fluorescent compound and quinone. Also used in dyes, as a hardener for dental restoration, for the determination of copper by spectrophotometric method, and for organic synthesis.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only

General References:

  1. Avasthi, Sushobhan, et al. Electronic structure and band alignment of 9, 10-phenanthrenequinone passivated silicon surfaces. Surface Science., 2011, 605 (13), 1308-1312.
  2. P L Chesis; D E Levin; M T Smith; L Ernster; B N Ames. Mutagenicity of quinones: pathways of metabolic activation and detoxification. PNAS, 1984, 81 (6), 1696-1700.
  3. Specific, highly sensitive reagent for arginine and arginyl peptides: Biochem. Biophys. Acta, 130, 538 (1966).
  4. Reagent for dehydrogenation, e.g. of thiazolines to thiazoles in high yield: J. Chem. Soc.(C), 1061 (1966). Review: Chem. Rev., 78, 317 (1978).
  5. Like 1,2-Cyclohexanedione, A14401, has been used by Ley's group for protection of trans-1,2-diols as cyclic diacetals. The method is particularly applicable to the carbohydrate field: Synlett, 793 (1996); J. Chem. Soc., Perkin 1, 2023 (1997):