Interesting facts
Interesting Facts about Naphthalene-1,5-diol
Naphthalene-1,5-diol, a fascinating aromatic compound, is known for its intriguing structure and diverse applications. Here are some interesting aspects that highlight its significance in the field of chemistry:
- Structural Features: Naphthalene-1,5-diol contains two hydroxyl groups (-OH) located on the 1st and 5th positions of the naphthalene ring system. This positioning impacts its chemical reactivity and interactions with other molecules.
- Reactivity: The presence of hydroxyl groups makes naphthalene-1,5-diol a potential candidate for various chemical reactions. It can participate in substitution reactions, leading to the creation of a wide array of derivatives.
- Applications: This compound is notable for its role in organic synthesis, where it can serve as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. Its derivatives have been explored for their biological activities.
- Biological Relevance: Some studies suggest that naphthalene-1,5-diol and its derivatives may exhibit antimicrobial properties, making them of interest in medicinal chemistry and potential therapeutic applications.
- Environmental Impact: Given its aromatic structure, understanding the environmental behavior of naphthalene-1,5-diol is crucial, especially concerning its persistence and degradation in natural systems.
- Research Playground: Naphthalene-1,5-diol is often used as a model compound in research to further investigate electrophilic aromatic substitution and the reactivity of hydroxylated naphthalene derivatives.
In summary, naphthalene-1,5-diol is not just a simple compound; it serves as a bridge between classic organic chemistry and modern applications, emphasizing the importance of understanding both its chemical properties and its role in various fields.
Synonyms
1,5-DIHYDROXYNAPHTHALENE
naphthalene-1,5-diol
83-56-7
1,5-Naphthalenediol
1,5-Dihydroxy naphthalene
Durafur Developer E
Oxidation Base
1,5-Dihydroxynapthalene
CI 76625
C.I. 76625
1,5-dihydroxynaphtalene
NSC 7202
EINECS 201-487-4
UNII-P25HC23VH6
MFCD00003980
BRN 2044951
DTXSID2052574
AI3-16636
NSC-7202
P25HC23VH6
1,5-NAPHTHOHYDROQUINONE
1,5-DIHYDROXYNAPHTHALINE
DTXCID9031147
EC 201-487-4
4-06-00-06554 (Beilstein Handbook Reference)
Azurol
1,5-Dihydroxynaphthaline; 1,5-Naphthohydroquinone; C.I. 76625; Durafur Developer E; NSC 7202; Oxidation Base
1,5Naphthalenediol
1,5-Naphthalindiol
1.5-naphthalenediol
Naphthalene-15-diol
1,5dihydroxynapthalene
1,5-dihydroxy-naphthalene
SCHEMBL28327
BIDD:GT0202
CHEMBL204658
1,5-Dihydroxynaphthalene, 97%
BDBM36287
NSC7202
1,5-NAPHTHALENEDIOL [INCI]
Tox21_303746
STL290515
AKOS005287408
FN67456
CAS-83-56-7
NCGC00357051-01
AC-11727
AS-12844
CS-0015800
D0590
NS00005084
EN300-52581
D72512
Q19842073
F0001-2128
Z276600344
Solubility of Naphthalene-1,5-Diol
Naphthalene-1,5-diol, with its chemical formula C10H8O2, is an intriguing compound when it comes to solubility characteristics. Its solubility can be influenced by several factors including temperature and the solvent used.
Solubility Characteristics:
In summary, while naphthalene-1,5-diol exhibits limited solubility in polar solvents like water, its solubility improves significantly in nonpolar organic solvents. Understanding these solubility properties is crucial for applications involving this compound.