Interesting facts
Interesting Facts About 6-Bromonaphthalen-2-ol
6-Bromonaphthalen-2-ol is a fascinating compound with various applications and unique characteristics that make it a subject of interest in both organic chemistry and material science. Here are some engaging facts about this chemical compound:
- Structural Features: This compound features a naphthalene ring system, which is fused and consists of two aromatic rings. The presence of the hydroxyl group (-OH) and the bromine atom (-Br) at specific positions creates a rich platform for further chemical reactivity.
- Reactivity: The hydroxyl group makes 6-bromonaphthalen-2-ol a good candidate for further substitution reactions. This allows chemists to explore functionalization of the naphthalene ring to develop new derivatives with tailored properties.
- Biological Activity: Compounds containing naphthalene systems have been studied for various biological activities. Some derivatives show potential antimicrobial or anti-inflammatory properties, making this area ripe for research.
- Industrial Applications: Naphthalene derivatives are often used as precursors in the synthesis of dyes, plastics, and pharmaceuticals. 6-Bromonaphthalen-2-ol may also find utility in the production of specialty chemicals.
- Research Interest: The compound is frequently used in the study of supramolecular chemistry, where it can interact with various substrates to form complex structures. These interactions can lead to novel material properties that are valuable in various applications.
As a compound with both theoretical and practical implications, 6-bromonaphthalen-2-ol provides an excellent opportunity for exploration in various fields of chemistry. Its unique structure and reactivity open doors for innovation and discovery that extend far beyond the laboratory.
Synonyms
6-Bromo-2-naphthol
15231-91-1
6-Bromo-2-naphthalenol
Bromo-6 naphtol-2
2-NAPHTHOL, 6-BROMO-
6-Bromo-beta-naphthol
87F10AHZ3O
NSC-17563
DTXSID5074551
CHEBI:34466
DTXCID5034935
239-279-0
6-bromonaphthalen-2-ol
2-Naphthalenol, 6-bromo-
6-Bromo2-hydroxynaphthalene
6-Bromo-naphthalen-2-ol
MFCD00004081
6-Bromo-.beta.-naphthol
6-bromonaphth-2-ol
2-bromo-6-hydroxynaphthalene
2-hydroxy-6-bromonaphthalene
6-bromo-2-hydroxynaphthalene
6-hydroxy-2-bromonaphthalene
F0701-0028
Bromo-6 naphtol-2 [French]
2-Bromo-6-naphthol
EINECS 239-279-0
NSC 17563
UNII-87F10AHZ3O
AI3-18464
6-bromo2-naphthol
6bromo-2-naphthol
6-bromo-2-naphtol
6-bromo-2-napthol
6-bromonapthalen-2-ol
6-bromonaphthalene-2-ol
6-bromo-naphthalene-2-ol
SCHEMBL49667
6-bromo- 2hydroxynaphthalene
6-Bromo-2-naphthol, 97%
BIDD:ER0052
2-bromo-6-hydroxy-naphthalene
2-hydroxy-6-bromo-naphthalene
orb1298098
SCHEMBL6105326
6-BROMO-2-NAPHTHALINOL
SCHEMBL30060950
HMS1651O22
SMSSF-0060169
NSC17563
STR02406
SBB054639
STL451630
AKOS000120485
CS-W001952
FB10626
HY-W001952
AC-12234
SY006200
TS-00535
DB-007128
B0621
NS00008279
ST45021341
EN300-17905
Q27116088
Z57074412
InChI=1/C10H7BrO/c11-9-3-1-8-6-10(12)4-2-7(8)5-9/h1-6,12
Solubility of 6-bromonaphthalen-2-ol
6-bromonaphthalen-2-ol, with the chemical formula C10H7BrO, exhibits interesting solubility characteristics primarily due to its unique molecular structure. Here’s what to note about its solubility:
In summary, while 6-bromonaphthalen-2-ol exhibits some solubility in polar solvents, it shows limited solubility in water. Understanding these solubility properties is crucial for its applications in chemical reactions and formulations.