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Thioridazine

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Identification
Molecular formula
C21H26N2S2
CAS number
50-52-2
IUPAC name
1-methyl-4-thioxanthen-9-ylidene-piperidine
State
State

At room temperature, thioridazine is in the solid state. Due to its form as a crystalline powder, it is stable under normal conditions but should be kept in a well-sealed container to prevent exposure to moisture and light.

Melting point (Celsius)
165.90
Melting point (Kelvin)
439.05
Boiling point (Celsius)
237.80
Boiling point (Kelvin)
510.95
General information
Molecular weight
370.58g/mol
Molar mass
370.5400g/mol
Density
1.3200g/cm3
Appearence

Thioridazine is typically encountered as a white to off-white crystalline powder. It can sometimes be observed in tablet form when formulated as a pharmaceutical product.

Comment on solubility

Solubility of 1-methyl-4-thioxanthen-9-ylidene-piperidine

The solubility of the compound 1-methyl-4-thioxanthen-9-ylidene-piperidine (C21H26N2S2) can be influenced by various factors, including temperature, solvent choice, and molecular structure. Understanding its solubility characteristics is crucial for applications in synthesis, formulation, and drug delivery.

Key Points on Solubility:

  • Solvent Polarity: The solubility of organic compounds often correlates with the polarity of the solvent used. Non-polar solvents like hexane may poorly dissolve polar compounds, while polar solvents like ethanol can significantly enhance solubility.
  • Molecular Interactions: The presence of functional groups such as thioether (thioxanthen) in the molecular structure can impact solubility due to its ability to engage in hydrogen bonding or van der Waals interactions with solvents.
  • Temperature Influence: Generally, increasing temperature raises solubility for many solids. However, for our compound, empirical studies are needed to determine the exact temperature effect.
  • Crystallinity: The degree of crystallinity in the compound can also play a role; amorphous forms tend to be more soluble than their crystalline counterparts.

In summary, while specific solubility data for 1-methyl-4-thioxanthen-9-ylidene-piperidine might be limited, the considerations above can guide future research and practical applications. As the compound is further studied, insights into its solubility behavior will undoubtedly emerge.

Interesting facts

Exploring 1-Methyl-4-Thioxanthen-9-Ylidene-Piperidine

1-Methyl-4-thioxanthen-9-ylidene-piperidine is a fascinating compound that captures the interest of chemists and researchers alike. Here are some intriguing aspects of this compound:

Unique Structural Features

  • Thioxanthene Core: The compound features a thioxanthene moiety, which is known for its rich chemistry and versatility in organic synthesis.
  • Piperidine Ring: The presence of the piperidine ring contributes to its potential biological activity, making it a subject of study in medicinal chemistry.
  • Methyl Substitution: The 1-methyl group introduces steric effects that may influence the compound's reactivity and interaction with biological targets.

Applications in Research

This compound has gained attention in several fields, particularly due to its potential applications:

  • Organic Synthesis: It can serve as an intermediate in the synthesis of more complex organic compounds.
  • Photodynamic Therapy: Its unique structure may allow it to be explored as a photosensitizer in cancer treatment.
  • Material Science: The properties of thioxanthenes have prompted investigations into their use in OLEDs (Organic Light Emitting Diodes).

In the Lab

Working with 1-methyl-4-thioxanthen-9-ylidene-piperidine opens up several experimental avenues, including:

  • Spectral Studies: Techniques such as NMR and UV-Vis spectroscopy can provide insights into its molecular structure and electronic properties.
  • Synthetic Pathways: Researchers might explore various synthetic routes to optimize yield and purity.
  • Biological Evaluation: Testing its interaction with biological systems can unveil potential therapeutic benefits.

In summary, 1-methyl-4-thioxanthen-9-ylidene-piperidine is more than just a compound; it embodies the beauty and complexity of organic chemistry, making it a valuable subject for both academic and practical investigations.

Synonyms
pimethixene
314-03-4
Calmixene
PIMETIXENE
Mepithiathene
Calmixen
Pimetixeno
Pimethixene [INN]
BP 400
Pimethixenum
1-methyl-4-thioxanthen-9-ylidenepiperidine
Pimethixenum [INN-Latin]
Pimetixeno [INN-Spanish]
1-methyl-4-(9H-thioxanthen-9-ylidene)piperidine
BP-400
9-(1-Methyl-4-piperidylidene)thioxanthene
EINECS 206-240-4
Calmixene (TN)
1-Methyl-4-(thioxanthen-9-ylidene)piperidine
Pimethixene (INN)
UNII-T46J20J26F
BRN 4143937
T46J20J26F
Piperidine, 1-methyl-4-thioxanthen-9-ylidene-
NSC-757828
PIMETHIXENE [MART.]
Piperidine, 1-methyl-4-(9H-thioxanthen-9-ylidene)-
PIMETHIXENE [WHO-DD]
CHEMBL152408
DTXSID0048476
NSC 757828
Pimethixenum (INN-Latin)
Pimetixeno (INN-Spanish)
PIMETHIXENE (MART.)
CAS-13187-06-9
Pimethixen
Pimethixene?
Spectrum_001324
Prestwick0_000294
Prestwick1_000294
Prestwick2_000294
Prestwick3_000294
Spectrum3_001441
Spectrum4_000424
Spectrum5_001353
Oprea1_122930
BSPBio_000228
BSPBio_002901
KBioGR_000748
KBioSS_001804
DivK1c_000432
SCHEMBL301596
SPBio_002447
BPBio1_000252
DTXCID0028450
CHEBI:94787
KBio1_000432
KBio2_001804
KBio2_004372
KBio2_006940
KBio3_002401
R06AX23
NINDS_000432
HY-B1101
BDBM50097224
AKOS015850901
CS-4692
DB13292
IDI1_000432
NCGC00016698-01
NCGC00016698-02
NCGC00016698-03
AC-13161
BS-49377
DA-56873
SBI-0051926.P002
1-methyl-4-(9-thioxanthenylidene)piperidine
1-Methyl-4-thioxanthen-9-ylidene-piperidine
AB00053710
NS00007237
D07406
E73927
AB00053710_06
EN300-18563908
Q6676377
BRD-K88090157-050-04-1
BRD-K88090157-050-06-6
BRD-K88090157-050-10-8
Piperidine, 1-methyl-4-(9H-thioxanthen-9-ylidene)-(9CI)
206-240-4