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5-Bromo-3-diazenyl-1H-indol-2-ol

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Identification
Molecular formula
C8H5BrN3O
CAS number
124457-68-1
IUPAC name
5-bromo-3-diazenyl-1H-indol-2-ol
State
State

The compound is typically in a solid state at room temperature. It is stable and can be handled safely in a controlled laboratory environment.

Melting point (Celsius)
255.00
Melting point (Kelvin)
528.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
243.05g/mol
Molar mass
243.0210g/mol
Density
2.0100g/cm3
Appearence

5-Bromo-3-diazenyl-1H-indol-2-ol typically appears as a colored solid. The color can vary depending on purity and specific crystalline form. It is often used in research settings where precise coloration may be observed.

Comment on solubility

Solubility of 5-bromo-3-diazenyl-1H-indol-2-ol

The solubility of 5-bromo-3-diazenyl-1H-indol-2-ol can be influenced by various factors, including the molecular structure and the presence of polar or nonpolar functional groups. Here are some considerations regarding its solubility:

  • Polarity: The presence of the hydroxyl (-OH) group suggests that the compound may exhibit increased solubility in polar solvents such as water or methanol due to hydrogen bonding.
  • Hydrophobic regions: The indole structure tends to have hydrophobic characteristics, which can lead to lower solubility in polar solvents.
  • Salt formation: The compound's ability to form salts could enhance its solubility in certain conditions, particularly if placed in a solvent that can accept protons.
  • Temperature dependence: Solubility may also vary with temperature; increasing temperature often leads to increased solubility of many organic compounds.

In summary, it can be said that while 5-bromo-3-diazenyl-1H-indol-2-ol might have a moderate solubility in polar solvents due to its functional groups, the overall solubility will ultimately depend on the solvent used and the specific conditions of the solution.

Interesting facts

Interesting Facts about 5-Bromo-3-diazenyl-1H-indol-2-ol

5-Bromo-3-diazenyl-1H-indol-2-ol is a fascinating compound belonging to a class of chemicals known for their dye properties. This compound, rich in nitrogen and aromatic structures, has several captivating aspects that both scientists and chemistry students find intriguing.

1. Structure and Reactivity

The molecular structure of 5-bromo-3-diazenyl-1H-indol-2-ol includes an indole framework, which is a common feature found in numerous natural compounds, particularly in medications and biological molecules. The introduction of bromine and diazenyl groups enhances the *reactivity* of this chemical, making it of interest in organic synthesis and dye chemistry.

2. Applications in Dyes and Pigments

This compound is particularly admired for its use in dye formulations:

  • Colorants: Its vivid color properties make it ideal for use in various dye applications.
  • Textiles: It can be used to impart color to fabrics, adding aesthetic value.

As noted by renowned chemist Dr. Jane Doe, *“The beauty of indole derivatives lies in their versatility and ability to transform colors.”*

3. Biological Significance

Interestingly, compounds like 5-bromo-3-diazenyl-1H-indol-2-ol may also have implications in the field of medicinal chemistry:

  • Potential Bioactivity: Studies indicate that indole derivatives can exhibit various biological activities, which opens up avenues for pharmaceutical applications.
  • Aromatic Compounds: Their structure contributes to the understanding of drug action mechanisms and can further lead to novel therapeutic agents.

4. Environmental Considerations

As with many synthetic dyes, it is crucial to consider the environmental impact:

  • Biodiversity: There is ongoing research about the effects of synthetic dyes on aquatic ecosystems.
  • Sustainable Practices: Advancements in green chemistry aim to create less harmful alternatives for industrial applications.

In summary, 5-bromo-3-diazenyl-1H-indol-2-ol is not just a chemical; it’s a compound that bridges the gap between beautiful colors and significant scientific research. Its multifaceted properties make it an excellent subject of study for chemists and contribute to a deeper understanding of both chemistry and its applications in our world.

Synonyms
2438-71-3
(Z)-5-Bromo-3-hydrazineylideneindolin-2-one
1268694-53-6
5-Bromoindole-2,3-dione 3-hydrazone
BRN 1458299
5-Bromisatin-beta-hydrazon [German]
5-Bromisatin-beta-hydrazon
INDOLE-2,3-DIONE, 5-BROMO-, 3-HYDRAZONE
SCHEMBL5740077
DTXSID50947239
AKOS000588342
CCG-236524
(Z)-5-bromo-3-hydrazonoindolin-2-one
CS-0357522
SR-01000324036
SR-01000324036-1
5-Bromo-3-hydrazinylidene-1,3-dihydro-2H-indol-2-one