2-Naphthalenol, 1-(phenylazo)-

• Formula: C₁₆H₁₂N₂O
• Molecular weight: 248.2793
• IUPAC Standard InChI: InChI=1S/C16H12N2O/c19-15-11-10-12-6-4-5-9-14(12)16(15)18-17-13-7-2-1-3-8-13/h1-11,19H Copy

  
• IUPAC Standard InChIKey: MRQIXHXHHPWVIL-UHFFFAOYSA-N Copy
• CAS Registry Number: 842-07-9
• 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: 1-Benzeneazo-2-naphthol; Benzeneazo-β-naphthol; Brasilazina Oil Orange; Calcogas Orange NC; Ceres Orange R; C.I. 12055; C.I. Solvent Yellow 14; Dispersol Yellow PP; Enial Orange I; Fast Oil Orange I; Fast Orange; Fat Orange 4A; Fat Orange G; Fat Orange I; Fat Orange R; Fat Orange RS; Fat Soluble Orange; Grasal Orange; Grasan Orange R; Hidaco Oil Orange; 2-Hydroxynaphthyl-1-azobenzene; 2-Hydroxy-1-phenylazonaphthalene; Lacquer Orange VG; Morton Orange Y; Oil Orange; Oil Orange 31; Oil Orange 2311; Oil Orange 2B; Oil Orange E; Oil Orange PEL; Oil Orange R; Oil Orange 7078-V; Oil Orange Z-7078; Oil Soluble Orange; Oleal Orange R; Orange Pel; Orange 3RA Soluble in Grease; Orange R Fat Soluble; Sudan I; Atul Orange R; Benzene-1-azo-2-naphthol; Brilliant Oil Orange R; Calco Oil Orange Z-7078; Calco Oil Orange 7078; Calco Oil Orange 7078-Y; Calcogas M; Campbelline Oil Orange; Carminaph; Cerotinorange G; Dunkelgelb; Fast Oil Orange; Fettorange lg; Fettorange R; Fettorange 4a; Motiorange R; NCI-C53929; Oil Orange EP; Oil Orange G; Oil Orange R-14; Orange A L'Huile; Orange Insoluble Olg; Orange Resenole No. 3; Orange Soluble A L'Huile; Organol Orange; Orient Oil Orange PS; Petrol Orange Y; Plastoresin Orange F4A; Pyronalorange; Resinol Orange R; Resoform Orange G; Sansel Orange G; Scharlach B; Silotras Orange TR; Solvent Yellow No. 14; Solvent Yellow 14; Somalia Orange I; Soudan I; Spirit Orange; Spirit Yellow I; Stearix Orange; Sudan J; Sudan Orange R; Sudan Orange RA; Sudan Orange RA New; Sudan Yellow; Sudan 1; Tertrogras Orange SV; Toyo Oil Orange; Waxakol Orange GL; Waxoline Yellow I; Waxoline Yellow IM; Waxoline Yellow IP; Waxoline Yellow IS; 1-(Phenylazo)-2-naphthalenol; 1-(Phenylazo)-2-naphthol; 1-Benzoazo-2-naphthol; 1-Phenylazo-β-naphthol; 2-Naphthol, 1-(phenylazo)-; 2-Naphtholazobenzene; Zlut rozpoustedlova 14; CI 12055; 2-Naphthalenol, 1-(2-phenyldiazenyl)-; Waxoline Orange EP-FW; 1-(2-Hydroxynaphthyl)azobenzene; 1-(Phenylazo)-2-hydroxynaphthalene; Disperse Yellow 97; α-Phenylazo-β-naphthol
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• Information on this page:
  • Reaction thermochemistry data
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
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Reaction 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

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

=

By formula: C₁₆H₁₂N₂O = C₁₆H₁₂N₂O

References

Go To: Top, Reaction thermochemistry data, Notes

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

Haessner, Mustroph, et al., 1985
Haessner, R.; Mustroph, H.; Borsdorf, R., H-NMR-spektroskopische Untersuchungen zur Azo-Hydrazon-Tautomerie in substituierten 1-Phenylazo-2-naphtholen, J. Prakt. Chem., 1985, 327, 555-566. [all data]

Notes

Go To: Top, Reaction thermochemistry data, References

• Symbols used in this document:
  

  ΔrH°	Enthalpy of reaction at standard conditions

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