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6-Bromo-1-methyl-2-naphthol

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Identification
Molecular formula
C11H9BrO
CAS number
18102-86-4
IUPAC name
6-bromo-1-methyl-naphthalen-2-ol
State
State

At room temperature, 6-Bromo-1-methyl-2-naphthol is in a solid state, characterized by its crystalline structure.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
237.09g/mol
Molar mass
237.0850g/mol
Density
1.4970g/cm3
Appearence

6-Bromo-1-methyl-2-naphthol typically appears as an off-white to beige crystalline solid. It has a notable aromatic odor characteristic of naphthalene derivatives.

Comment on solubility

Solubility of 6-bromo-1-methyl-naphthalen-2-ol

The solubility of 6-bromo-1-methyl-naphthalen-2-ol can be understood through its chemical structure and characteristics. This compound is primarily a non-polar substance due to the presence of the naphthalene ring, which influences its ability to dissolve in different solvents.

Key points about its solubility include:

  • Generally insoluble in water due to its hydrophobic naphthalene structure.
  • Soluble in non-polar organic solvents such as hexane, benzene, and chloroform.
  • Lower solubility observed in polar solvents compared to non-polar ones.

In summary, the solubility of 6-bromo-1-methyl-naphthalen-2-ol exhibits a notable preference for non-polar environments, making it more amenable to dissolution in organic solvents rather than in aqueous solutions. This property is critical for its applications in organic synthesis and further research into its behavior in different chemical contexts.

Interesting facts

Interesting Facts About 6-Bromo-1-methyl-naphthalen-2-ol

6-Bromo-1-methyl-naphthalen-2-ol is a fascinating compound that finds its applications in various fields of chemistry and materials science. Here are some engaging insights:

  • Structural Significance: This compound features a naphthalene backbone, a structure renowned for its stability and hydrophobic characteristics. The presence of the −Br group introduces interesting reactivity and alters its chemical properties.
  • Biological Relevance: Compounds like 6-bromo-1-methyl-naphthalen-2-ol often show biological activity, which may be harnessed in pharmaceuticals or agrochemicals. Researchers are keen on exploring such halogenated naphthalenes for potential medicinal properties.
  • Applications in Organic Synthesis: This compound can serve as an intermediate in organic synthesis, particularly in the development of more complex molecules. Its reactivity may allow for various transformations, enhancing the toolkit of synthetic chemists.
  • Environmental Impact: As environmental concerns increase, the study of halogenated compounds like 6-bromo-1-methyl-naphthalen-2-ol becomes critical. Understanding its degradation pathways and toxicity contributes to safer industrial practices.
  • Analytical Techniques: This compound often serves as a subject for analytical chemistry techniques, such as chromatography and spectroscopy. These methods help in understanding its behavior in different environments and applications.

In summary, 6-bromo-1-methyl-naphthalen-2-ol exemplifies the intricate relationship between structure and function in organic compounds. As research continues, the potential applications and implications of this compound in various scientific fields remain an exciting area of study.

Synonyms
1-Methyl-6-bromo-2-naphthol
2-NAPHTHOL, 6-BROMO-1-METHYL-
16667-01-9
BRN 3243936
DTXSID20168151
3-06-00-03020 (Beilstein Handbook Reference)
DTXCID3090642
6-bromo-1-methylnaphthalen-2-ol
6-Bromo-1-methyl-2-naphthol
SCHEMBL5343236
SCHEMBL31444547
YNZVWWALVATSDE-UHFFFAOYSA-N
MFCD01712261
SY468661