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1,3-Dimethylindoline-2-thione

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Identification
Molecular formula
C10H11NS
CAS number
38224-59-2
IUPAC name
1,3-dimethylindoline-2-thione
State
State

At room temperature, 1,3-dimethylindoline-2-thione is typically in a solid state. It is usually handled under standard laboratory conditions due to its stability in solid form.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
318.00
Boiling point (Kelvin)
591.15
General information
Molecular weight
177.28g/mol
Molar mass
177.2760g/mol
Density
1.1605g/cm3
Appearence

1,3-Dimethylindoline-2-thione typically appears as a crystalline solid. It may present colors ranging from yellowish to light brown, depending on its specific state and purity.

Comment on solubility

Solubility of 1,3-Dimethylindoline-2-thione

1,3-Dimethylindoline-2-thione is an intriguing compound when it comes to its solubility characteristics. Understanding its solubility can provide insights into its chemical behavior and potential applications. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound tends to be soluble in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and chloroform.
  • Water Solubility: The solubility in water is relatively low, which is common for many organic compounds with similar structures.
  • Temperature Influence: The solubility may increase with temperature, suggesting that heating the solvent could enhance dissolution rates.
  • pH Sensitivity: Changes in pH can influence solubility, so it may be more soluble in acidic or basic conditions depending on the ionization states.

As chemical scientists often say, "Solubility is the key to reactivity." This means that understanding how well 1,3-dimethylindoline-2-thione dissolves in various media can greatly impact its reactivity and application in chemical processes. Therefore, future studies exploring its solubility in differing environments can yield further valuable insights.

Interesting facts

Interesting Facts about 1,3-Dimethylindoline-2-thione

1,3-Dimethylindoline-2-thione is a fascinating compound that holds significance in various scientific domains. Here are some key points that highlight its importance:

  • Unique Structure: The molecule features an indoline backbone, which is characterized by a fused ring structure. This gives it unique chemical properties and potential reactivity.
  • Thione Functional Group: The presence of a thione (-C=S) group contributes to its reactivity and allows for intriguing applications in chemistry.
  • Application in Dyes: Compounds like 1,3-dimethylindoline-2-thione are often used in the dye industry owing to their vibrant color properties, making them valuable in textiles and plastics.
  • Potential Biological Activity: Research suggests that thione compounds may exhibit significant biological activities, including antibacterial and antifungal properties, rendering them useful in medicinal chemistry.
  • Versatile Intermediates: This compound can serve as an important intermediate in organic synthesis, providing a basis for the creation of more complex chemical entities.

Overall, 1,3-dimethylindoline-2-thione exemplifies how seemingly simple compounds can play crucial roles in various applications, bridging gaps between basic research and practical uses in industries.

Synonyms
13637-41-7
2H-Indole-2-thione, 1,3-dihydro-1,3-dimethyl-
BRN 1527851
1,3-Dimethyl-2-indolinethione
2-INDOLINETHIONE, 1,3-DIMETHYL-
1,3-Dihydro-1,3-dimethyl-2H-indole-2-thione
5-21-08-00080 (Beilstein Handbook Reference)
1-methyl-3-methylthiooxindole
CHEMBL346029
SCHEMBL11438801
DTXSID80929346
TYFJUZPJHYOUES-UHFFFAOYSA-N
1,3-dimethyl-1,3-dihydro-2H-indole-2-thione