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1-methyl-3-nitrosoindole-2-ol

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Identification
Molecular formula
C9H8N2O2
CAS number
1708-56-7
IUPAC name
1-methyl-3-nitroso-indol-2-ol
State
State

The compound is typically in a solid state at room temperature, exhibiting crystalline characteristics.

Melting point (Celsius)
112.00
Melting point (Kelvin)
385.15
Boiling point (Celsius)
311.00
Boiling point (Kelvin)
584.15
General information
Molecular weight
176.18g/mol
Molar mass
176.1780g/mol
Density
1.3400g/cm3
Appearence

1-Methyl-3-nitrosoindole-2-ol typically appears as a crystalline solid. The compound exhibits a distinctive coloration typical of nitroso compounds, which can range from yellowish to brown.

Comment on solubility

Solubility of 1-methyl-3-nitroso-indol-2-ol

The solubility of the compound 1-methyl-3-nitroso-indol-2-ol can be influenced by several factors, including its molecular structure and the solvent used.

Generally, the compound exhibits varying degrees of solubility in different solvents:

  • Polar Solvents: This compound is likely to have reasonable solubility in polar solvents such as water or ethanol due to the presence of hydroxyl groups which facilitate hydrogen bonding.
  • Non-Polar Solvents: In non-polar solvents, the solubility may be significantly lower due to the lack of polar interactions.

It is important to note that the overall solubility can be affected by temperature, concentration, and the presence of other ions or molecules in the solution.

In summary, while 1-methyl-3-nitroso-indol-2-ol shows favorable solubility characteristics in polar environments, the specific solubility parameters should be determined through experimental methods to accurately gauge its behavior in various conditions.

Interesting facts

Interesting Facts about 1-methyl-3-nitroso-indol-2-ol

1-methyl-3-nitroso-indol-2-ol is an intriguing compound that offers a wealth of interesting characteristics and applications. Here are some noteworthy facts:

  • Biological Significance: This compound is part of the indole family, which is renowned for its wide array of biological activities. Indoles play essential roles in various natural processes and are often found in numerous biologically active compounds.
  • Potential Therapeutic Uses: Research has indicated that compounds related to indole structures can possess anticancer, anti-inflammatory, and antimicrobial properties. This opens up pathways for new medicinal applications.
  • Stability and Reactivity: The nitroso group in 1-methyl-3-nitroso-indol-2-ol makes it a subject of study in terms of its stability under different conditions. The compound's reactivity can lead to various chemical transformations, making it significant in synthetic organic chemistry.
  • Research Applications: This compound can be employed as a probe in chemical and biological analyses. Its unique structure allows chemists to study interactions at the molecular level, contributing to our understanding of organic reactions.
  • Indole Framework: The indole backbone is a versatile structure, often used in the synthesis of dyes, pigments, and pharmaceuticals. The incorporation of a nitroso group adds unique reactivity, making derivatives of this compound appealing for laboratory research.

In conclusion, 1-methyl-3-nitroso-indol-2-ol exemplifies the complexity and potential of indole-based compounds in various fields. Whether in medicinal chemistry or organic synthesis, its unique characteristics continue to inspire scientists and researchers alike.

Synonyms
3265-24-5
(Z)-3-(Hydroxyimino)-1-methylindolin-2-one
1-Methylindole-2,3-dione 3-oxime
1-methyl-3-nitrosoindol-2-ol
(3E)-3-hydroxyimino-1-methylindol-2-one
INDOLE-2,3-DIONE, 1-METHYL-, 3-OXIME
1-methyl-1H-indole-2,3-dione 3-oxime
1-Methylisatin oxime
Isatin, 1-methyl-, 3-oxime
N-Methyl-isatin-3-oxim [German]
N-Methyl-isatin-3-oxim
N-methylisatin 3-oxime
N-Methyl-isatin-3-oxime
SCHEMBL5194860
XVDVCPOWCPQHNC-NTMALXAHSA-N
DTXSID701291972
HMS1667A12
1-methyl-2,3-indoledione 3-oxime
STK794587
AKOS001589781
AKOS002684276
AKOS030229642
SB65102
(3Z)-1-Methyl-1H-indole-2,3-dione 3-oxime
(3Z)-1-Methyl-1H-indole-2,3-dione 3-oxime #
AG-690/33035030
(3E)-3-HYDROXYIMINO-1-METHYL-INDOL-2-ONE
Z49568662
(3Z)-3-(hydroxyimino)-1-methyl-1,3-dihydro-2H-indol-2-one
3-HYDROXYIMINO-1-METHYL-1,3-DIHYDRO-2H-INDOL-2-ONE