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1-Nitrosoindoline

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Identification
Molecular formula
C8H8N2O
CAS number
16042-14-9
IUPAC name
1-nitrosoindoline
State
State

1-Nitrosoindoline is in a solid state at room temperature, usually appearing in powder or crystalline forms.

Melting point (Celsius)
111.00
Melting point (Kelvin)
384.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
148.16g/mol
Molar mass
148.1580g/mol
Density
1.2646g/cm3
Appearence

1-Nitrosoindoline is typically a yellow crystalline solid, often found in powdered form. It is sensitive to light and may degrade upon prolonged exposure.

Comment on solubility

Solubility of 1-nitrosoindoline

1-nitrosoindoline, with the chemical formula C9H8N2O, displays intriguing solubility characteristics that are influenced by its unique structural properties. Understanding its solubility behavior is crucial for applications in various chemical processes. Here are some key insights:

  • Solvent Compatibility: 1-nitrosoindoline is generally soluble in organic solvents. Commonly used solvents include:
    • Acetone
    • Ethyl acetate
    • Dichloromethane
  • Limited Water Solubility: The compound exhibits poor solubility in water. This limited solubility can affect its behavior in aqueous environments, making it essential to consider alternative solvents for specific applications.
  • Temperature Dependence: As with many organic compounds, the solubility of 1-nitrosoindoline may increase with temperature, enabling greater dissolution in organic solvents when heated.

In summary, while 1-nitrosoindoline shows promising solubility in several organic solvents, its low solubility in water necessitates careful solvent selection in laboratory and industrial processes.

Interesting facts

Interesting Facts about 1-nitrosoindoline

1-nitrosoindoline is a fascinating chemical compound that has garnered attention in various fields of study due to its unique properties and applications. Here are some intriguing points about this compound:

  • Chemical Structure: The presence of a nitroso group (-NO) attached to an indoline framework gives 1-nitrosoindoline its distinctive properties and reactivity. This structure plays a critical role in its interaction with biological systems.
  • Reactivity: 1-nitrosoindoline is known for its electrophilic nature, making it an important reagent in organic synthesis. It is particularly useful in the preparation of various derivatives.
  • Biological Activity: Some studies have suggested that 1-nitrosoindoline may exhibit biological activities, which could open avenues for research in medicinal chemistry.
  • Analytical Applications: The compound has been utilized in analytical chemistry to detect specific target molecules owing to its reactive properties.
  • Historical Significance: Compounds containing the indoline structure have been of interest since the late 19th century, showcasing the rich history of research in this area of chemistry.

As researchers continue to explore its applications, 1-nitrosoindoline stands as a testament to the creative nature of chemistry, where every molecule tells its own story and contributes to advancements in science and technology. Remember, as the renowned chemist Linus Pauling famously said, "The best way to have a good idea is to have lots of ideas." This principle can be applied as we delve deeper into the properties and potential of 1-nitrosoindoline!

Synonyms
1-Nitrosoindoline
7633-57-0
N-Nitrosoindoline
1-Nitroso-2,3-dihydro-1H-indole
INDOLINE, 1-NITROSO-
N-Nitrosoindolin
1-nitroso-2,3-dihydroindole
N-Nitrosoindolin [German]
BRN 0132426
N-Nitroso-indolin
1-Nitrosoindoline #
5-20-06-00250 (Beilstein Handbook Reference)
CHEMBL351284
SCHEMBL2344277
DTXSID00227194
Indole, 2,3-dihydro-N-nitroso-
HAA63357
AKOS004905091
SB65956
BS-29533
G10012
EN300-7375456
Z1198156346