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
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • References
  • Notes
• Other data available:
  • 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

IR Spectrum

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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: Coblentz Society, Inc.

Condensed Phase Spectrum

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Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. More information on the manner in which spectra in this collection were collected can be found here.

Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.

Additional Data

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

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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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