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1,4-Dihydroxy-5,8-tetrahydronaphthalene

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Identification
Molecular formula
C10H12O2
CAS number
490-91-5
IUPAC name
4a,5,8,8a-tetrahydronaphthalene-1,4-dione
State
State

At room temperature, 1,4-Dihydroxy-5,8-tetrahydronaphthalene is a solid.

Melting point (Celsius)
133.00
Melting point (Kelvin)
406.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
176.20g/mol
Molar mass
176.1980g/mol
Density
1.3060g/cm3
Appearence

This compound is typically found as yellow crystalline powder.

Comment on solubility

Solubility of 4a,5,8,8a-tetrahydronaphthalene-1,4-dione

The solubility of 4a,5,8,8a-tetrahydronaphthalene-1,4-dione is influenced by its structural characteristics and the nature of its interactions with solvents. It is crucial to consider the following factors:

  • Polarity: The compound tends to be moderately polar due to the presence of the dione functional groups, which can engage in hydrogen bonding.
  • Solvent Interaction: This compound is generally soluble in organic solvents like ethanol and acetone, but its solubility in water is limited.
  • Temperature Effects: Increasing temperature can enhance solubility in organic solvents due to the endothermic nature of dissolution.

In summary, while 4a,5,8,8a-tetrahydronaphthalene-1,4-dione exhibits some degree of solubility in polar organic solvents, it is not readily soluble in water.

Understanding the solubility characteristics of such compounds is essential for their application in various chemical processes.

Interesting facts

Interesting Facts About 4a,5,8,8a-Tetrahydronaphthalene-1,4-dione

4a,5,8,8a-tetrahydronaphthalene-1,4-dione is a fascinating organic compound that plays a significant role in various fields of chemistry. Here are some intriguing aspects of this compound:

  • Structural Beauty: The compound features a unique bicyclic structure, which is notable for its fused rings. This configuration contributes to its interesting chemical behavior and reactivity.
  • Biological Relevance: Compounds like 4a,5,8,8a-tetrahydronaphthalene-1,4-dione are often studied for their potential biological activities. Their structure might allow them to interact with a variety of biological targets, making them candidates for pharmaceutical research.
  • Synthetic Versatility: The synthesis of this compound can provide insights into synthetic strategies used in organic chemistry. It often serves as an intermediate in the synthesis of more complex molecules, showcasing the flexibility of synthetic approaches.
  • Reaction Pathways: The presence of carbonyl groups in its structure allows this compound to participate in a range of chemical reactions, including reductions and electrophilic substitutions, which are fundamental concepts taught in organic chemistry courses.
  • Material Applications: Such compounds may have implications in materials science, particularly in the development of organic semiconductors or other advanced materials due to their unique electronic properties.

In sum, 4a,5,8,8a-tetrahydronaphthalene-1,4-dione is not just a molecule with a complex name; it embodies a rich landscape of chemical potential waiting to be explored. Whether in synthesis, biological applications, or material sciences, this compound captivates the curiosity of scientists and students alike.

Synonyms
4a,5,8,8a-Tetrahydro-1,4-naphthoquinone
6271-40-5
4a,5,8,8a-tetrahydronaphthalene-1,4-dione
1,4-Naphthalenedione, 4a,5,8,8a-tetrahydro-
NSC 36727
4A,5,8,8a-Tetrahydro-[1,4]naphthoquinone
NSC36727
1,4-NAPHTHOQUINONE, 4a,5,8,8a-TETRAHYDRO-
1, 4a,5,8,8a-tetrahydro-
SCHEMBL10399375
RLUZSEVUJQNQNV-UHFFFAOYSA-N
WLN: L66 BV EV CU HUTJ
35043-92-6
NSC-36727
NSC155659
1, 4a,5,8,8a-tetrahydro-, cis-
NSC-155659
4a,8,8a-Tetrahydro-1,4-naphthoquinone
cis-4a,8,8a-Tetrahydro-1,4-naphthoquinone
4a, 5, 8, 8a-tetrahydro-1,4-naphtoquinone
1,4,4a,5,8,8a-hexahydronaphthalene-1,4-dione