Skip to main content

1,6-dibromonaphthalen-2-ol

ADVERTISEMENT
Identification
Molecular formula
C10H6Br2O
CAS number
15974-86-6
IUPAC name
1,6-dibromonaphthalen-2-ol
State
State

At room temperature, 1,6-dibromonaphthalen-2-ol is in a solid state. It is known for its stability under normal conditions.

Melting point (Celsius)
123.00
Melting point (Kelvin)
396.15
Boiling point (Celsius)
434.50
Boiling point (Kelvin)
707.65
General information
Molecular weight
330.96g/mol
Molar mass
330.9630g/mol
Density
2.1696g/cm3
Appearence

1,6-Dibromonaphthalen-2-ol typically appears as a crystalline solid. The compound may exhibit a color ranging from off-white to a light yellow, depending on its purity and the presence of any impurities.

Comment on solubility

Solubility of 1,6-Dibromonaphthalen-2-ol

The solubility of 1,6-dibromonaphthalen-2-ol in various solvents can vary significantly due to its unique molecular structure and the presence of functional groups.

Key Points about Solubility:

  • Polar Solvents: This compound is likely to have limited solubility in highly polar solvents, such as water, due to its large hydrophobic naphthalene rings.
  • Non-Polar Solvents: It tends to be more soluble in non-polar solvents like hexane or toluene, where the hydrophobic interactions are favorable.
  • Comparative Solubility: Compared to simpler alcohols or bromonaphthalene derivatives, 1,6-dibromonaphthalen-2-ol may exhibit distinct solubility behaviors influenced by intermolecular interactions.

In key studies, solubility is often evaluated under specific conditions, and it is crucial to recognize that temperature, pressure, and the presence of other solutes can significantly impact solubility outcomes. As such, the general notion might be summarized as: "the solubility is a balance between polar and non-polar interactions." Similarly, insights from formulations and practical applications illustrate that 1,6-dibromonaphthalen-2-ol could serve as an effective component in non-polar solvents.

Interesting facts

Interesting Facts about 1,6-Dibromonaphthalen-2-ol

1,6-Dibromonaphthalen-2-ol is a fascinating organic compound with remarkable characteristics that capture the interest of chemists and researchers alike. Below are some intriguing facets about this compound:

  • Structural Composition: This compound features a naphthalene ring, which is a bicyclic structure composed of two fused benzene rings. The presence of bromine atoms, along with a hydroxyl (-OH) group, significantly influences its chemical behavior.
  • Applications in Research: The unique properties of 1,6-dibromonaphthalen-2-ol make it an important area of study in organic synthesis and material science. Researchers are particularly interested in its applications as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.
  • Biological Relevance: Some studies suggest that derivatives of naphthalene compounds may exhibit antibacterial properties. This potential opens pathways for further investigation into the biological activity of 1,6-dibromonaphthalen-2-ol and its derivatives.
  • Substituent Variability: The presence of different substituents (like bromine and hydroxyl) allows for a diverse range of chemical behavior. This compound can readily participate in further substitution reactions, making it a versatile building block in organic chemistry.
  • Environmental Considerations: Like many brominated compounds, there are considerations regarding the environmental impact of 1,6-dibromonaphthalen-2-ol. Understanding its degradation pathways and toxicity is crucial for developing safer chemical processes.

In summary, 1,6-dibromonaphthalen-2-ol stands out as a compound of significant interest in the realms of chemistry and biology. As one researcher aptly put it, “Every compound tells a story; it is our job to read between the lines.” With ongoing research, the story of this compound continues to unfold, revealing its potential in diverse applications.

Synonyms
1,6-Dibromo-2-naphthol
16239-18-2
2-Naphthalenol, 1,6-dibromo-
2-NAPHTHOL, 1,6-DIBROMO-
1,6-Dibromo-beta-naphthol
AI3-19853
NSC 9870
EINECS 240-356-6
BRN 2092298
1,6-DIBROMO-2-NAPHTHALENOL
DTXSID0075100
1,6-Dibromonaphthalen-2-ol methanol monosolvate
1,6Dibromobetanaphthol
2Naphthol, 1,6dibromo
2Naphthalenol, 1,6dibromo
DTXCID7035220
240-356-6
1,6-dibromonaphthalen-2-ol
1,6-Dibromo-2-hydroxynaphthalene
C10H6Br2O
MFCD00003870
1,6-Dibromo-.beta.-naphthol
2-Hydroxy-1,6-dibromonaphthalene
NSC-9870
NSC9870
2-Naphthol,6-dibromo-
1,6 Dibromo-2-napthol
2-Naphthalenol,6-dibromo-
W9S75P5MUJ
SCHEMBL50832
1,6-dibromo-naphthalen-2-ol
WLN: L66J BE CQ HE
VKESFYLPKHQOOA-UHFFFAOYSA-
SBB043714
STK084906
AKOS000274066
AC-22895
DS-16396
ST029626
SY051565
CS-0097759
D1872
NS00025303
EN300-170624
SR-01000312287
SR-01000312287-1
InChI=1/C10H6Br2O/c11-7-2-3-8-6(5-7)1-4-9(13)10(8)12/h1-5,13H