Interesting facts
Interesting Facts About 1-nitrosonaphthalen-2-ol
1-nitrosonaphthalen-2-ol is a fascinating compound that draws attention not only for its unique structure but also for its diverse applications in the field of chemistry. Here are some engaging insights about this compound:
- Unique Nitration: This compound contains a nitroso group (-NO) attached to a naphthalene ring, which is a polycyclic aromatic hydrocarbon. The positioning of the nitroso group plays a crucial role in the compound's reactivity and interaction with other substances.
- Biological Significance: 1-nitrosonaphthalen-2-ol has been studied for its potential biological activities. Research indicates that compounds with a nitroso group can exhibit various pharmacological effects, making this compound of interest in medicinal chemistry.
- Intermediate in Synthesis: It serves as an important intermediate in organic synthesis. Chemists often leverage such compounds to create more complex molecules, thus facilitating the development of various pharmaceuticals and agrochemicals.
- Environmental Considerations: As with many nitrated organic compounds, 1-nitrosonaphthalen-2-ol may be involved in reactions that can impact environmental chemistry. Its behavior in various environments is crucial for understanding pollution and toxicity.
In summary, the study of 1-nitrosonaphthalen-2-ol exemplifies the intricate connections between structure and functionality in organic chemistry. Its unique properties not only make it a subject of scientific inquiry but also a valuable tool for synthetic chemists.
Synonyms
1-Nitroso-2-naphthol
131-91-9
1-nitrosonaphthalen-2-ol
2-Naphthalenol, 1-nitroso-
2-Naphthol, 1-nitroso-
Nitroso-beta-naphthol
1-Nitroso-2-naftol
Zelen moridlova 4
Zelen moridlova 4 [Czech]
2636-79-5
Nitroso-.beta.-naphthol
alpha-Nitroso-beta-naphthol
NSC 4151
1-Nitroso-2-naftol [Czech]
CCRIS 1556
1,2-Naphthalenedione, 1-oxime
1-NITROSO-2-NAPHTHALENOL
alpha-Nitroso-beta-naftol
alpha-Nitroso-beta-naftol [Czech]
C.I. 10000
EINECS 205-043-0
MFCD00003884
BRN 0776947
AI3-09078
(E)-1-(hydroxyimino)naphthalen-2(1H)-one
757I55U2QX
NSC-4151
DTXSID9059622
.alpha.-Nitroso-.beta.-naphthol
4-07-00-02419 (Beilstein Handbook Reference)
1-NITROSO-2-NAPHTHOL [MI]
NSC677525
1-(hydroxyimino)naphthalen-2(1H)-one
(1E)-1-(hydroxyimino)naphthalen-2(1H)-one
1,2-Naphthoquinone 1-oxime
UNII-757I55U2QX
1Nitroso2naftol
Nitrosobetanaphthol
alphaNitrosobetanaftol
2Naphthol, 1nitroso
.alpha.-Nitroso-.beta.-naphthol oxime
.alpha.-Nitrosonaphthol
2Naphthalenol, 1nitroso
1-nitrosonaphthalene-2-ol
1-nitroso-naphthalen-2-ol
1,2-naphthoquinone-1-oxime
WLN: L66J BNO CQ
SCHEMBL103998
.alpha.-Nitroso-.beta.-naftol
1-Nitroso-2-naphthol, 97%
SCHEMBL8947876
DTXCID5034014
DTXSID30876194
NSC4151
CAQHPYSDQFDJAL-KHPPLWFESA-N
CHEBI:194993
1-Nitroso-2-naphthol, 98.0%
BDBM108228
BBL000016
BBL011067
NSC107835
STK391542
STK802252
AKOS000283071
AKOS005622627
AKOS006279793
FN34396
NSC-107835
NSC-677525
AC-18344
AS-15422
DB-042070
CS-0336127
N0266
NS00013464
EN300-21463
H11769
AE-562/40186369
Q3596764
1-Nitroso-2-naphthol, SAJ special grade, >=97.0%
1‐nitroso‐2‐naphthol (Substrate 5)
205-043-0
Solubility of 1-nitrosonaphthalen-2-ol
1-nitrosonaphthalen-2-ol, with its unique structure, presents some interesting characteristics regarding its solubility. This compound, featuring both a nitroso and an alcohol group, exhibits variable solubility depending on the solvent used:
As a result, one could state the solubility behavior can be summarized as:
Understanding the solubility of this compound is crucial for its application in various fields, especially in organic synthesis and material science, where effective solvation can significantly affect reaction outcomes.