Promazine

• Formula: C₁₇H₂₀N₂S
• Molecular weight: 284.419
• IUPAC Standard InChI: InChI=1S/C17H20N2S/c1-18(2)12-7-13-19-14-8-3-5-10-16(14)20-17-11-6-4-9-15(17)19/h3-6,8-11H,7,12-13H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: ZGUGWUXLJSTTMA-UHFFFAOYSA-N Copy
• CAS Registry Number: 58-40-2
• 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: 10H-Phenothiazine-10-propanamine, N,N-dimethyl-; Phenothiazine, 10-[3-(dimethylamino)propyl]-; A 145; Ampazine; Berophen; Esparin; Liranol; N-[3-(Dimethylamino)propyl]phenothiazine; Neo-Hibernex; Prazin; Prazine; Promwill; Protactyl; Romtiazin; RP 3276; Sinophenin; Tomil; Verophen; Wy 1094; 10-[3-(Dimethylamino)Propyl]phenothiazine; 3276 R. P.; N-Dimethylamino-1-methylethyl thiodiphenylamine; Promazin; Promazina; NSC 31447; Phenothiazine, 10-(1-dimethylaminopropyl)-; Sparine; N,N-Dimethyl-3-(10H-phenothiazin-10-yl)-1-propanamine
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Gas phase ion energetics 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:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

Ionization energy determinations

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.

Poltorakov, Pirnazarova, et al., 1973
Poltorakov, A.P.; Pirnazarova, F.N.; But, P.G.; Piruzyan, L.A.; Chibrikin, V.M.; Vikjlyaev, Yu.I.; Ul'yanova, O.V., Ionization potentials of phenothiazine derivatives and their correlation with the parmacologic effect, Bull. Acad. Sci. USSR, Div. Chem. Sci., 1973, 22, 2050, In original 2106. [all data]

Fulton and Lyons, 1968
Fulton, A.; Lyons, L.E., The ionization energies of some phenothiazine tranquillizers and molecules of similar structure, Australian J. Chem., 1968, 21, 873. [all data]

Domelsmith, Munchausen, et al., 1977
Domelsmith, L.N.; Munchausen, L.L.; Houk, K.N., Photoelectron spectra of psychotropic drugs. 2. Phenothiazine and related tranquilizers, J. Am. Chem. Soc., 1977, 99, 6506. [all data]

Notes

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