2-Naphthalenol, acetate

• Formula: C₁₂H₁₀O₂
• Molecular weight: 186.2066
• IUPAC Standard InChI: InChI=1S/C12H10O2/c1-9(13)14-12-7-6-10-4-2-3-5-11(10)8-12/h2-8H,1H3 Copy

  
• IUPAC Standard InChIKey: RJNPPEUAJCEUPV-UHFFFAOYSA-N Copy
• CAS Registry Number: 1523-11-1
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: 2-Naphthol, acetate; β-Naphthol acetate; β-Naphthyl acetate; Naphthalene, 2-acetoxy-; O-Acetyl-β-naphthol; 2-Acetoxynaphthalene; 2-Naphthyl acetate; Acetic acid β-naphthyl ester; 2-Naphthalenol, 2-acetate; NSC 37069
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• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • Mass spectrum (electron ionization)
  • References
  • Notes
• Other data available:
  • Gas Chromatography
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Condensed phase thermochemistry data

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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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Phase change data

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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 as indicated in comments:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

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

References

Go To: Top, Condensed phase thermochemistry data, Phase change data, Mass spectrum (electron ionization), Notes

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

Colomina, Roux, et al., 1975
Colomina, M.; Roux, M.V.; Turrion, C., Thermochemical properties of naphthalene compounds III. Enthalpies of combustion and formation of the 1- and 2-naphthylacetic acids and 1- and 2-naphthyl acetates, J. Chem. Thermodyn., 1975, 7, 759-762. [all data]

Leman and Lepoutre, 1948
Leman, A.; Lepoutre, G., Chaleurs de combustion des naphtols, C. R. Acad. Sci. Paris, 1948, 226, 1976-19. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Khetarpal, Lal, et al., 1981
Khetarpal, S.C.; Lal, K.; Bhatnagar, H.L., Indian J. Chem., 1981, 446. [all data]

VEREVKIN, ROUX, et al., 2003
VEREVKIN, SERGEY P.; ROUX, MARIA VICTORIA; NOTARIO, RAFAEL; DEMASTERS, DOUGLAS E.; LIEBMAN, JOEL F., The energetics of naphthalene derivatives. II. The isomeric 1--- and 2---naphthyl acetates, Molecular Physics, 2003, 101, 21, 3231-3237, https://doi.org/10.1080/00268970310001620195 . [all data]

Bystrom, 1981
Bystrom, K., Enthalpies of combustion, vaporization, and formation for di-n-propyldiazene N-oxide and di-t-butyldiazene N-oxide, J. Chem. Thermodyn., 1981, 13, 139-145. [all data]

Notes

Go To: Top, Condensed phase thermochemistry data, Phase change data, Mass spectrum (electron ionization), References

• Symbols used in this document:
  

  Tfus	Fusion (melting) point
  ΔcH°solid	Enthalpy of combustion of solid at standard conditions
  ΔfH°solid	Enthalpy of formation of solid at standard conditions
  ΔfusH	Enthalpy of fusion
  ΔsubH°	Enthalpy of sublimation at standard conditions

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