Prochlorperazine

• Formula: C₂₀H₂₄ClN₃S
• Molecular weight: 373.943
• IUPAC Standard InChI: InChI=1S/C20H24ClN3S/c1-22-11-13-23(14-12-22)9-4-10-24-17-5-2-3-6-19(17)25-20-8-7-16(21)15-18(20)24/h2-3,5-8,15H,4,9-14H2,1H3 Copy

  
• IUPAC Standard InChIKey: WIKYUJGCLQQFNW-UHFFFAOYSA-N Copy
• CAS Registry Number: 58-38-8
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: 10H-Phenothiazine, 2-chloro-10-[3-(4-methyl-1-piperazinyl)propyl]-; Phenothiazine, 2-chloro-10-[3-(4-methyl-1-piperazinyl)propyl]-; Bayer A 173; Capazine; Chlormeprazine; Chlorperazine; Compazine; Emelent; Kronocin; Meterazin; Meterazine; Nipodal; Prochlorpemazine; Prochlorperazin; Prochlorpromazine; Procloperazine; Proclorperazine; Stemetil; SKF 4657; Tementil; Temetid; 6140 R.P.; Chloro-3 (N-methylpiperazinyl-3 propyl)-10 phenothiazine; 2-Chloro-10-(3-(1-methyl-4-piperazinyl)-propyl)-phenothiazine; 2-Chloro-10-(3-(4-methyl-1-piperazinyl)propyl)phenothiazine; 3-Chloro-10-(3-(1-methyl-4-piperazinyl)propyl)phenothiazine; N-(γ-(4'-Methylpiperazinyl-1')propyl)-3-chlorophenothiazine; Novamin; Prochloroperazine; 6140 RP; RP-6140; Phenothiazine, 2-chloro-10-[3-(1-methyl-4-piperazinyl)propyl]-; Proazine
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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]

Notes

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