Benzo[b]thiophene, 2-(2-naphthalenyl)-

• Formula: C₁₈H₁₂S
• Molecular weight: 260.353
• IUPAC Standard InChI: InChI=1S/C18H12S/c1-2-6-14-11-16(10-9-13(14)5-1)18-12-15-7-3-4-8-17(15)19-18/h1-12H Copy

  
• IUPAC Standard InChIKey: VXNMJAGOXHIGRF-UHFFFAOYSA-N Copy
• CAS Registry Number: 17164-77-1
• Chemical structure:
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• Other names: Benzo[b]thiophene, 2-(2-naphthyl)-; 2-(2-Naphthyl)benzo[b]thiophene; 2-(2-Naphthyl)-1-thiaindene; 2-(2-Naphthyl)-1-benzothiophene; 2-(2-Naphthalenyl)benzo[b]thiophene; 2-(2'-naphthyl)-benzo[b]thiophene; 2-(2-Naphthyl)benzothiophene
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• Information on this page:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Lee's RI, non-polar column, temperature ramp

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Lee's RI, non-polar column, custom temperature program

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Vassilaros, Kong, et al., 1982
Vassilaros, D.L.; Kong, R.C.; Later, D.W.; Lee, M.L., Linear retention index system for polycyclic aromatic compounds. Critical evaluation and additional indices, J. Chromatogr., 1982, 252, 1-20, https://doi.org/10.1016/S0021-9673(01)88394-1 . [all data]

Lee, Vassilaros, et al., 1979
Lee, M.L.; Vassilaros, D.L.; White, C.M.; Novotny, M., Retention Indices for Programmed-Temperature Capillary-Column Gas Chromatography of Polycyclic Aromatic Hydrocarbons, Anal. Chem., 1979, 51, 6, 768-773, https://doi.org/10.1021/ac50042a043 . [all data]

Brack and Schirmer, 2003
Brack, W.; Schirmer, K., Effect-directed identification of oxygen and sulfur heterocycles as major polycyclic aromatic cytochrome P4501A-inducers in a contaminated sedimet, Environ. Sci. Technol., 2003, 37, 14, 3062-3070, https://doi.org/10.1021/es020248j . [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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