Interesting facts
Interesting Facts about Naphthalene-1,2-dione
Naphthalene-1,2-dione, known for its unique structure and properties, is an intriguing compound in the field of organic chemistry. Here are some captivating aspects of this compound:
- Structural Significance: Naphthalene-1,2-dione features a quinonoid structure, which is a key characteristic that distinguishes it from other aromatic compounds. This structure plays a significant role in its reactivity and potential applications.
- Reactivity: The presence of the diketone functional groups allows naphthalene-1,2-dione to undergo various chemical reactions, including nucleophilic additions and redox reactions. Its reactivity makes it an interesting subject for synthetic chemistry.
- Biological Activity: Some studies suggest that naphthalene-1,2-dione exhibits biological activities such as antimicrobial and antitumor properties. This has piqued the interest of researchers in drug development and medicinal chemistry.
- Industrial Applications: Due to its chemical characteristics, naphthalene-1,2-dione is utilized in the production of dyes, pigments, and as an intermediate in various chemical syntheses. This versatility makes it valuable in both academic research and industrial applications.
- Historical Relevance: The study of naphthalene derivatives dates back to the early 19th century, highlighting the long-standing significance of naphthalene-1,2-dione in chemical research and its evolution over the years.
In conclusion, naphthalene-1,2-dione is not just a simple compound; its multifaceted properties and applications make it a vital component of numerous scientific inquiries and industrial endeavors. As stated by chemists, "Each compound tells a story, and naphthalene-1,2-dione's narrative is rich with potential and discovery."
Synonyms
1,2-NAPHTHOQUINONE
524-42-5
1,2-Naphthalenedione
o-Naphthoquinone
beta-Naphthoquinone
1,2-Naphthaquinone
.beta.-Naphthoquinone
1,2-Naftochinon
ortho-naphthoquinone
1,2-Naftochinon [Czech]
1,2-dihydronaphthalene-1,2-dione
1,2-Dihydro-1,2-diketo-naphthalene
CCRIS 1558
HSDB 2036
NSC 9831
EINECS 208-360-2
BRN 0606546
CHEBI:34055
AI3-14930
NSC-9831
804K62F61Q
NAPHTHOQUINONE, 1,2-
DTXSID2060171
1,2-NAPHTHOQUINONE [MI]
1,2-NAPHTHOQUINONE [HSDB]
4-07-00-02417 (Beilstein Handbook Reference)
oNaphthoquinone
betaNaphthoquinone
1,2Naftochinon
1,2Naphthaquinone
1,2naphthalenedione
1,2Dihydro1,2diketonaphthalene
DTXCID6041189
208-360-2
naphthalene-1,2-dione
MFCD00001698
CHEMBL52347
MLS000069467
SMR000059112
UNII-804K62F61Q
orthonaphthoquinone
ortho-1
Naphthoquinone-(1,2)
Opera_ID_1388
WLN: L66 BVVJ
1,2-Naphthoquinone, 97%
cid_10667
SCHEMBL173316
1,2-Dione-Based Compound, 8
BDBM22851
NSC9831
1,2-Naphthoquinone, technical grade
BBL027354
STK581215
AKOS003588995
AKOS025243285
FN01989
AC-15181
AS-48267
PD147991
SY033798
DB-005062
N0041
NS00032507
EN300-31420
F30116
Q171721
Z324553598
Solubility of Naphthalene-1,2-dione
Naphthalene-1,2-dione, with the chemical formula C10H8O2, presents interesting solubility characteristics that are worth noting. This compound is known to be relatively insoluble in water due to its non-polar aromatic structure. However, solubility can vary significantly in different solvents:
Overall, the solubility of naphthalene-1,2-dione is a critical factor to consider in various chemical processes. As the saying goes, “like dissolves like,” and in this case, its affinity for non-polar solvents highlights the essential nature of solvent selection in chemical reactions and applications.
Understanding the solubility of this compound can greatly influence its utility in synthesis and other chemical endeavors.