Interesting facts
Interesting Facts about 1-Nitronaphthalen-2-ol
1-Nitronaphthalen-2-ol, often abbreviated as 1-NO, is a fascinating compound that combines the properties of both nitro and hydroxyl functional groups. Below are some notable aspects of this interesting chemical:
- Structural Significance: This compound features a nitro group (-NO2) and a hydroxy group (-OH) on the naphthalene ring, positioning these groups at the 1 and 2 positions, respectively. This creates an environment ripe for a variety of chemical reactions.
- Functional Versatility: Due to the presence of different functional groups, 1-NO can participate in various reactions such as electrophilic substitution and nucleophilic addition, making it a valuable intermediate in organic synthesis.
- Biological Relevance: Compounds like 1-nitronaphthalene derivatives have been studied for their potential biological activity, including roles in medicinal chemistry. Some derivatives exhibit antibacterial or anti-inflammatory properties, opening avenues for pharmaceutical research.
- Environmental Considerations: The nitro group in 1-NO can render it less stable under certain conditions, affecting its persistence in the environment. Understanding its degradation pathways is essential for assessing its environmental impact.
- Colorimetric Applications: Like many naphthalene derivatives, 1-NO can serve as a colorimetric agent, which allows for the detection of specific ions in analytical chemistry.
In summary, the unique combination of nitro and hydroxyl functionalities in 1-nitronaphthalen-2-ol not only contributes to its intriguing chemical behavior but also underlines its importance in various scientific fields, including organic synthesis, medicinal chemistry, and environmental science. As scientists continue to explore its properties, 1-NO may reveal even more applications yet to be discovered.
Synonyms
1-Nitro-2-naphthol
550-60-7
2-Naphthalenol, 1-nitro-
1-Nitro-2-hydroxynaphthalene
1-Nitro-2-naphthalenol
2-NAPHTHOL, 1-NITRO-
1-Nitro-beta-naphthol
alpha-Nitro-beta-naphthol
CCRIS 1555
.alpha.-Nitro-.beta.-naphthol
1-Nitro-.beta.-naphthol
EINECS 208-984-5
UNII-29IRK301OW
NSC 37027
BRN 2050005
29IRK301OW
NSC-37027
DTXSID10203540
1-NITRO-2-NAPHTHOL [MI]
NITRO-2-NAPHTHALENOL, 1-
4-06-00-04307 (Beilstein Handbook Reference)
DTXCID40126031
2-Naphthalenol, 1-nitro-(9CI)
208-984-5
sshivhkmgvbxtj-uhfffaoysa-n
1-nitronaphthalen-2-ol
2-Hydroxy-1-nitronaphthalene
NSC37027
MFCD00021461
1-nitro-naphthalen-2-ol
SCHEMBL767775
AKOS024261037
AS-57750
DB-052680
CS-0146754
N0370
NS00033238
EN300-383968
T72604
Q27254430
Solubility of 1-Nitronaphthalen-2-ol
1-Nitronaphthalen-2-ol, with the chemical formula C10H9NO2, exhibits particular solubility characteristics that are crucial for its applications in chemical synthesis and research. The solubility of this compound can be influenced by several factors:
In conclusion, while 1-nitronaphthalen-2-ol shows moderate solubility in polar solvents, its behavior in non-polar environments may lead to minimal dissolution. It is essential for practicing chemists to consider these factors, as they can significantly impact both the handling and reactivity of this intriguing compound.