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N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline

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Identification
Molecular formula
C14H14ClNS
CAS number
51423-28-2
IUPAC name
N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline
State
State

This compound is in a solid state at room temperature.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
371.10
Boiling point (Kelvin)
644.25
General information
Molecular weight
263.80g/mol
Molar mass
263.8030g/mol
Density
1.3070g/cm3
Appearence

The compound generally appears as a crystalline solid.

Comment on solubility

Solubility of N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline

N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline, a compound with potential applications in various chemical processes, displays interesting solubility characteristics. The solubility of this compound is influenced by several factors:

  • Polarity: The presence of the sulfanyl group can enhance the overall polarity of the molecule, potentially increasing its solubility in polar solvents.
  • Functional Groups: The chlorophenyl group contributes to varying degrees of solubility based on the environment, affecting how it interacts with solvents.
  • Solvent Effects: This compound is more likely to dissolve in solvents such as ethanol or dichloromethane, which can stabilize polar functional groups.
  • Temperature Dependence: As with many organic compounds, solubility may increase with rising temperatures, allowing greater interaction with solvent molecules.

In general, understanding the solubility of N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline is crucial for effective application in synthetic chemistry and material science. Due to the intricate balance of its functional groups, the solubility behavior can vary significantly and should be tested in practical scenarios.

Interesting facts

Exploring N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline

N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline, often referred to in research as a sulfonamide compound, has intriguing properties and applications that are noteworthy for both chemists and pharmaceutical scientists. Here are some fascinating insights into this compound:

  • Role in Synthesis: This compound contains a sulfenyl group, which can play a pivotal role in various synthetic methodologies, particularly in the design of new pharmaceuticals and materials.
  • Biological Activities: Compounds with an aniline backbone are known for their biological activities, making them potential candidates in drug discovery. Investigations into this compound may reveal useful pharmacological properties.
  • Chlorine Substitution Effects: The presence of a chlorophenyl group could enhance lipophilicity and membrane permeability, which are essential for bioactivity. The chlorine atom's electron-withdrawing properties can also affect the compound's reactivity.
  • Research Interest: This compound has garnered attention in fields like medicinal chemistry and material science due to its unique structure, which blends aromatic and aliphatic characteristics.
  • Potential Applications: Applications might be explored in areas such as:
    • Pharmaceuticals - as a building block for drug development
    • Material Sciences - in creating polymers or chemical sensors

In summary, N-[(4-chlorophenyl)sulfanylmethyl]-N-methyl-aniline stands out due to its unique structural features and potential applications. As quoted by many researchers, "Understanding the nuances of compound interaction in medicinal chemistry can lead to breakthroughs in treatment paradigms." Further studies and explorations are essential to unlock its full potential!

Synonyms
956-06-9
ANILINE, N-(((p-CHLOROPHENYL)THIO)METHYL)-N-METHYL-
N-(((p-Chlorophenyl)thio)methyl)-N-methylaniline
N-[[(p-Chlorophenyl)thio]methyl]-N-methylaniline
Aniline, N-[[(p-chlorophenyl)thio]methyl]-N-methyl-
NSC 89483
BRN 2735340
NSC89483
NCIOpen2_005547
WLN: GR DS1N1&R
4-12-00-00301 (Beilstein Handbook Reference)
DTXSID90241889
NSC-89483